WO2007007288A2 - Ensemble de maquillage et/ou de soin cosmetique - Google Patents

Ensemble de maquillage et/ou de soin cosmetique Download PDF

Info

Publication number
WO2007007288A2
WO2007007288A2 PCT/IB2006/052392 IB2006052392W WO2007007288A2 WO 2007007288 A2 WO2007007288 A2 WO 2007007288A2 IB 2006052392 W IB2006052392 W IB 2006052392W WO 2007007288 A2 WO2007007288 A2 WO 2007007288A2
Authority
WO
WIPO (PCT)
Prior art keywords
oil
acid
composition
assembly
weight
Prior art date
Application number
PCT/IB2006/052392
Other languages
English (en)
Other versions
WO2007007288A3 (fr
Inventor
Xavier Blin
Original Assignee
L'oreal
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FR0552204A external-priority patent/FR2888475B1/fr
Application filed by L'oreal filed Critical L'oreal
Publication of WO2007007288A2 publication Critical patent/WO2007007288A2/fr
Publication of WO2007007288A3 publication Critical patent/WO2007007288A3/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06—Lipsticks

Definitions

  • the present invention relates to a cosmetic makeup and/or care assembly for keratin materials and to a makeup process using said assembly.
  • the assemblies toward which the present invention is directed are more particularly intended for applying makeup and/or care products to the skin, the lips and/or the integuments.
  • These products are especially lipsticks, lip balms, lip pencils, liquid or solid foundations, especially cast as a stick or a dish, concealer products and skin coloring products, temporary tattoos, eye makeup products, for instance eye liners, in particular in the form of pencils, mascaras or eyeshadows.
  • eye makeup products for instance eye liners, in particular in the form of pencils, mascaras or eyeshadows.
  • one subject of the invention is a makeup assembly for caring for and/or making up keratin materials, comprising at least:
  • composition placed inside said compartment, the composition comprising at least one fatty phase and consisting of at least 50% by weight of compound(s) approved for food use.
  • a subject of the invention is an assembly for caring for and/or making up keratin material(s), comprising at least:
  • composition comprising at least one aqueous phase and consisting of at least 50% by weight of compound(s) approved for food use relative to its total weight.
  • the compounds approved for food use may be "food grade compounds”.
  • the process of the invention may be a make up process.
  • application means associated with the container is intended to denote application means sold with the container, preferably inside the same overall or primary packaging.
  • the application means and the container may be coupled in various ways.
  • the application means may be securely fastened to the container, and especially to a means for closing off an aperture of the container.
  • the application means are securely fastened to the part of the container delimiting the compartment containing the composition.
  • the application means may be arranged inside the container, optionally in contact with the composition inside the compartment, without, however, being securely fastened to any of the constituents of the container.
  • the invention relates to a makeup patch for a support chosen from the skin, the lips and the integuments, comprising at least one composition in accordance with the invention.
  • a subject of the invention is a cosmetic process for caring for and/or making up keratin materials, comprising the application, on contact with a keratin material, of the composition packaged in an assembly according to the invention.
  • the compositions packaged according to the invention contain a physiologically acceptable medium.
  • composition denotes a composition as defined in Directive 93/35/EEC of the Council of 14 June 1993.
  • physiologically acceptable medium denotes a nontoxic medium that may be applied to at least one human keratin material.
  • keratin materials covers the skin, mucous membranes, for instance the lips, the nails and keratin fibers, such as the eyelashes and the hair.
  • the cosmetic compositions in accordance with the present invention are particularly advantageous for use on the skin and the lips.
  • COMPOUNDS APPROVED FOR FOOD USE More generally, according to the invention, the term "compounds approved for food use” means compounds chosen from ozokerite, rice wax, compounds referenced in the Codex alimentarius and materials consisting exclusively of compounds referenced in the Codex alimentarius, for example such as pearls.
  • the Codex Alimentarius, or Food Code is the world reference acting as the authority for consumers, producers and processors of foodstuffs, national food control bodies and the international food products market.
  • a compound referenced in the Codex alimentarius denotes a compound whose use as a food ingredient is considered in the Codex, and is or is not regulated therein according to specific terms. It is understood that when terms are specified in the Codex alimentarius for certain ingredients, they are not decisive for the implementation of these same compounds in the compositions according to the invention.
  • the term “food” ingredient denotes any substance other than water, used in the manufacture or preparation of a food and present in the finished product even though occasionally in a modified form.
  • the term “food ingredient” especially includes food additives and food extracts.
  • the term "food additive” means any substance that is not normally consumed as a foodstuff per se and is not normally used as a characteristic ingredient of a food, whether or not it has nutrient value, and whose deliberate addition to the foodstuff for a technological or organoleptic purpose, at any step in the manufacture, transformation, preparation, processing, packaging, wrapping, transportation or storage of this foodstuff, leads or may lead (directly or indirectly) to its incorporation or to the incorporation of derivatives thereof into the foodstuff or can affect in any other way the characteristics of this foodstuff.
  • a product consisting exclusively of compounds referenced in the Codex alimentarius denotes a material whose composition consists exclusively of compounds referenced in the Codex alimentarius and which, consequently, comprises at least two compounds, or even more, referenced in the Codex alimentarius.
  • Materials of multilayer structure for instance pearls, are especially covered under this definition.
  • pearls generally consist of a mineral substrate such as mica or TiO 2 covered, for example, with a coat of iron oxide.
  • extracts are especially defined in the Codex alimentarius volume 8 and more particularly in the Codex standards 19, 33 and 210.
  • the Codex under consideration is the version of the Codex standard 210 as amended in 2003.
  • the Codex As regards edible fats and oils, the Codex under consideration is the version of the Codex standard 19-1981, as revised in February 1993. For example, for olive oil, reference may be made more particularly to the version of Codex standard 33, revised in 1989.
  • the "compounds approved for food use” according to the present invention are “food grade compounds”.
  • a “food grade compound” may be a "compound approved for food use” that is sold as food grade compounds, i.e. a compound for which the supplier states it can be used in a food product.
  • a food grade compound is a compound specifically made to match the needs of the food industry.
  • a food grade compound can consist only of edible products.
  • a "food grade compound” can also refers to a compound, specifications of which are given in the US Code of Federal Regulation Title 21 Chap I Parts 73, 74, 82, 172, 184 and 854.
  • each chemical compound is defined as a "food grade compound” by a specification comprising i) a chemical name, ii) impurity levels the compound can contain, and/or iii) the concentration at which it can be used in a food.
  • the food grade compound will be used in the cosmetic composition with the specifications given in US Code of Federal Regulation Title 21 Chap I.
  • the part under consideration is 184.
  • the parts under consideration are 172, 73, 74 and 82.
  • compositions in accordance with the invention comprise at least 50% by weight, especially at least 55% by weight or even at least 60% by weight, in particular at least 65% by weight, and more particularly at least 70% by weight and especially at least 75% by weight, or even at least 80% by weight, especially at least 85% by weight, in particular at least 90% by weight, especially at least 95% by weight and more particularly consist of about 100% by weight of compound(s) approved for food use relative to their total weight.
  • the compositions in accordance with the invention comprise at least 50% by weight, in particular at least 60% by weight, especially at least 70% by weight, especially at least 80% by weight, especially at least 90% by weight, and more particularly consist of about 100% by weight, relative to their total weight, of food grade compound(s).
  • the presence of the compounds under consideration according to the invention does not prove to be harmful to the expected associated qualities for a cosmetic composition, for example as regards wear or gloss in the case of lipsticks, or covering power in the more particular case of foundations.
  • the assembly of the application means conventionally used in cosmetics is able to be suitable insofar as these means lend themselves to application to the keratin material for which the composition is intended.
  • these application means may be securely fastened to or independent from the container also composing the assembly according to the invention.
  • the application means may be securely fastened to a closing member for sealing off (or sealing member) an aperture of the container.
  • the application unit may be formed at the end of a member, for example of elongated stem type, connecting the application unit to the sealing member.
  • the application unit may be in the form of a coarse brush, a comb, a fine brush, a felt, a sinter, an open-cell or closed-cell foam, a feather, a tip or a spatula.
  • This application unit may be porous, for example fibrous, hairy or tubular, or in the form of a wand (such as for applying traditional kohl).
  • the application unit may be chosen especially from cotton tips, foam tips, felt tips, flocked tips, ceramic tips or a sinter material and pads.
  • the application unit may also be a coarse brush, a comb, a fine brush, a sponge, a foam, a fountain pen, a tubular-tipped pen, a pad or a hollow stem in order especially to allow application to the lips, the eyelashes, the eyebrows, the hair or the nails.
  • the application unit may, where appropriate, have abrasive properties.
  • the application means of an assembly in accordance with the invention may include a unit securely fastened to the container.
  • This securely fastened unit may be, for example, in the form of a block of foam, a sinter, a system of roll-on type or a perforated wall.
  • the unit may comprise at least one surface intended to come into contact with the keratin materials so as to allow the application of the composition in accordance with the invention to these materials.
  • the surface of the application unit liable to come into contact with the keratin materials may be in permanent or selective communication with the composition in accordance with the invention placed inside the container.
  • the application means may be independent from the container.
  • they may consist of a support, especially in the form of a patch, a wipe, a pad or a glove.
  • composition according to the invention may be placed on and/or inside the support, especially by impregnation or by any deposition means usually used in the field.
  • the support may have a surface, especially a flocked surface, intended to come into contact with the composition in order to take up an amount of this composition so as to apply it to the keratin materials.
  • the flocking methods and the materials used for flocking are those usually used in the field.
  • the supports used in the present invention may be of any nature, and in particular those used in cosmetics.
  • the support may be in the form of a patch.
  • patch means a structure in the form of a monolayer or multilayer sheet or web, comprising a matrix in which may be incorporated at least one composition in accordance with the invention, which is capable, when the matrix is placed in contact with a substrate, especially the skin, of partially releasing the composition. After a certain leave-on time, the patch is removed and all or some of the composition initially contained in the matrix has become transferred to the support, especially by evaporation or transfer.
  • This patch may or may not be dry.
  • a diluent may either be furnished with the patch, or provided directly by the user. It may be, for example, water or a biological secretion from the user, for instance saliva and sweat secretions.
  • the patches according to the invention may also advantageously be in the form of stencils or stamps, which have the advantage of being able to be preconditioned in terms of forms to create novel patterns on the surface to be made up.
  • it may be a two-sheet patch, between which is contained a splitable capsule of liquid, which is broken only at the time of application. The liquid released then impregnates the face of the patch that is against the targeted support.
  • It may also be a patch equipped with a solar sensor that can especially allow the temperature to be increased.
  • the patch may be of the coated paper type, especially as described in French patent application FR 0 309 301.
  • the matrix of the patch may comprise at least one gelling polymer chosen from: celluloses, and especially modified celluloses, for instance hydroxyethylcellulose modified with a cetyl chain, such as Natrosol Plus ® sold by the company Hercules, crosslinked ethyltrimethylammonium methacrylate chloride homopolymers, especially as an inverse emulsion in a mineral oil, for instance the product sold by the company Ciba under the trade name Salcare SC 95 ® , polyacrylamidotauramide homopolymers, especially in the form of the sodium salt thereof (AMPS), in particular as an inverse emulsion, for instance Simulgel 800 ® sold by the company SEPPIC, and mixtures thereof.
  • celluloses and especially modified celluloses, for instance hydroxyethylcellulose modified with a cetyl chain, such as Natrosol Plus ® sold by the company Hercules, crosslinked ethyltrimethylammonium methacrylate chloride homopolymers
  • the application time may vary over a wide range and may range from a few seconds to several hours or overnight.
  • the matrix may be deposited on a support capable of promoting its handling and/or of optionally producing an occlusive or semiocclusive barrier. This support may be fixed with an adhesive or a holding device to stay in place and allow a pattern to be drawn.
  • the support may comprise a cavity into which at least one part of the human body may be inserted.
  • the support may have, for example, the form of a glove, especially a mitten, thus allowing the support to be applied to a hand, or to be used as a glove for treating other parts of the body.
  • the support may advantageously be in varied forms, each adapted to a particular use. Thus, it may be in the form of a finger stall, a bonnet for covering the head, in order to treat the hair or the scalp, or a bag intended to be placed around an ear.
  • the cavity may be made from a single sheet of folded support or from several sheets of support assembled together, for example by welding, bonding or sewing.
  • the support When the support is intended to be applied to at least part of the face, it may have at least one aperture, for example for the eyes, the nose and/or the mouth.
  • the application unit may be formed from the composition itself.
  • the composition may be in the form of a solid wand, placed inside a case formed by the container.
  • the container may advantageously be equipped with a mechanism capable of moving the wand from a first position, in which it is arranged essentially inside the case, to a second position in which at least part of the wand emerges from the case through an aperture such that an application surface of the solid wand is outside the case to allow the application of the composition to the keratin materials.
  • the emerged part of the wand formed from the composition according to the invention itself constitutes an application unit.
  • composition it may be formulated in any form of container, generally selected to be compatible with the preparation and the type of application means selected. It may especially be a container capable of constituting a reservoir for said composition, for example a tube, a jar or a dish, as illustrated, for example, in figure 1.
  • the container of an assembly in accordance with the invention may, where appropriate, be equipped with a draining unit through which the application unit is intended to pass, at least when the application unit is removed from the container, so as to dose the amount of compositions present on the application unit.
  • a draining unit through which the application unit is intended to pass, at least when the application unit is removed from the container, so as to dose the amount of compositions present on the application unit.
  • the application member may include a vibrating source to make it vibrate.
  • the assembly according to the invention may also comprise means delimiting at least one given motif which are suitable for applying the composition.
  • these means may be in the form of piece(s), such as cutouts, motifs or friezes, and, in particular, may be of the stencil type.
  • the stencils may be in the form of bands, friezes, for example in the form of a roll from which the desired length is unwound and which the user can position on the areas to be made up by selecting the length to be applied in order to obtain the personalized decorative effect.
  • these means may form an integral part of the application means.
  • composition in accordance with the invention packaged in a device suitable for application of said composition in the form of premounted motifs.
  • the assembly may comprise a plurality of containers, for example in the form of a plurality of trays or sachets, for example which may be linked together via splitable zones.
  • the cosmetic compositions packaged according to the present invention may comprise a fatty phase especially comprising at least one compound chosen from oils and fatty substances that are solid at room temperature (20 - 25°C) and atmospheric pressure, for example such as waxes and pasty fatty substances, and mixtures thereof. Oils and solid fatty substances and mixtures thereof in a form suitable for human consumption, whether or not they have been subjected to conversions such as transesterification, hydrogenation or fractionation, are thus most particularly suitable for the invention.
  • Oils and solid fatty substances are especially foodstuffs in accordance with the definition in section 1 of the Codex alimentarius and composed of fatty acid glycerides.
  • the oils and solid fatty substances are food grade compounds. They are more particularly listed in the US Code of Federal Regulation Title 21 Chap I Parts 172, 184 and 854.
  • They may be of animal, plant, mineral, synthetic or marine origin.
  • lipids may contain a small amount of other lipids, for instance phosphatides, unsaponifiable constituents and free fatty acids naturally present in these solid fatty substances and oils.
  • oil means any fatty substance that is in liquid form at room temperature (20 - 25°C) and atmospheric pressure.
  • the liquid fatty phase may also contain, besides oils, other compounds dissolved in the oils, such as gelling and/or structuring agents.
  • the cosmetic composition according to the present invention may comprise at least one and in particular at least two oils.
  • the oils that are suitable for the preparation of the cosmetic compositions according to the invention may be volatile or nonvolatile oils.
  • volatile oil means an oil (or nonaqueous medium) capable of evaporating on contact with the skin in less than one hour, at room temperature and atmospheric pressure.
  • the volatile oil is a volatile cosmetic oil, which is liquid at room temperature, especially having a nonzero vapor pressure, at room temperature and atmospheric pressure, in particular having a vapor pressure ranging from 0.13 Pa to 40 000 Pa (10 ⁇ 3 to 300 mmHg), preferably ranging from 1.3 Pa to 13 000 Pa (0.01 to lOO mmHg) and preferably ranging from 1.3 Pa to 1300 Pa (0.01 to
  • nonvolatile oil means an oil
  • the volatile or nonvolatile oils may be hydrocarbon-based oils especially of animal, mineral or plant origin, synthetic oils, silicone oils or fluoro oils, or mixtures thereof.
  • hydrocarbon-based oil means an oil mainly containing hydrogen and carbon atoms and possibly oxygen, nitrogen, sulfur and/or phosphorus atoms.
  • the oils that are more particularly considered according to the invention are hydrocarbon-based oils and more preferentially edible oils especially referenced in the Codex alimentarius and more specifically in standards 19 to 27, 33, 34, 123 to 128 and 210 thereof.
  • oils comprising at least one fatty acid chosen from caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, ricinoleic acid, linoleic acid, linolenic acid, arachidic acid, gadoleic acid, behenic acid, erucic acid, brassidic acid, cetoleic acid, lignoce
  • hydrocarbon-based plant oils are more particularly hydrocarbon-based plant oils and in particular those chosen from triglycerides consisting of fatty acid esters of glycerol, the fatty acids of which may have chain lengths ranging from C 4 to C 24 , these chains possibly being linear or branched, and saturated or unsaturated.
  • oils are especially heptanoic or octanoic triglycerides, groundnut oil, babassu oil, coconut oil, grapeseed oil, cottonseed oil, corn oil, corn germ oil, mustard seed oil, palm oil, rapeseed oil, sesame seed oil, soybean oil, sunflower oil, wheatgerm oil, canola oil, apricot oil, mango oil, castor oil, shea oil, avocado oil, olive oil, sweet almond oil, peach kernel oil, walnut oil, hazelnut oil, macadamia oil, jojoba oil, alfalfa oil, poppy seed oil, pumpkin oil, marrow oil, blackcurrant oil, evening primrose oil, millet oil, barley oil, quinoa oil, rye oil, safflower oil, candlenut oil, passionflower oil, musk rose oil or shea butter oil, or alternatively caprylic/capric acid triglycerides, and mixtures thereof.
  • compositions according to the instant invention will contain at least some canola oil, in particular when they are intended to confer a gloss effect.
  • compositions according to the invention will contain reduced amounts of castor oil.
  • the castor oil is inclined to be partially oxidized by air with time and thus may generate unpleasant smell.
  • the compositions may preferably contain less than 5% by weight of castor oil, especially less than 2%, in particular less than 1% by weight relative to the total weight of the composition and more particularly are free of castor oil.
  • the cosmetic compositions in accordance with the invention may comprise at least one oil chosen from hydrocarbon- based plant oils and more particularly chosen from the following oils approved for food use: isopropyl myristate sold by Stearinerie Dubois, the caprylic/capric acid triglycerides sold by Stepan; hybrid rapeseed oil, liquid cottonseed oil, refined protected deodorized mango oil, the liquid fraction of protected shea butter and the refined canola seed oil sold by Karlshamns; Lipex Sheasoft and cottonseed oil sold by Karslshamns; the deodorized apricot kernel oil sold by Nestle; the sweet almond oil sold by Soetenaey; the peach kernel oil sold by Aarhus United; rapeseed oil, corn germ oil, olive oil, grapeseed oil, soybean oil and sunflower oil sold by Huileries de Lapalisse and walnut oil sold by Soetenaey.
  • isopropyl myristate sold by Stearinerie Dubois the caprylic/
  • these oil compounds are food grade compounds, as defined previously in the application.
  • the cosmetic composition in accordance with the present invention comprises at least one oil chosen from canola oil, caprylic/capric acid triglycerides, apricot oil, peach oil, walnut oil and olive oil.
  • the cosmetic compositions according to the invention comprise from 0.1% to 99% by weight, especially from 1% to 90% by weight, in particular from 5% to 70% by weight, in particular from 10% to 65% by weight and more particularly from 20% to 60% by weight, relative to the total weight of oil(s) approved for food use in the composition and more particularly referenced in the Codex alimentarius.
  • compositions in accordance with the present invention may obviously comprise at least one other liquid fatty substance, with the proviso that it is present in amounts in accordance with the requirements according to the invention.
  • Nonvolatile hydrocarbon-based oils that may especially be mentioned include: synthetic ethers containing from 10 to 40 carbon atoms; linear or branched hydrocarbons of mineral or synthetic origin such as petroleum jelly, polydecenes, hydrogenated polyisobutene such as Parleam, and squalane, and mixtures thereof, and in particular hydrogenated polyisobutene, synthetic esters, for instance oils of formula R 1 COOR 2 in which R 1 represents a linear or branched fatty acid residue containing from 1 to 40 carbon atoms and R 2 represents a hydrocarbon-based chain that is especially branched, containing from 1 to 40 carbon atoms provided that R 1 + R 2 > 10.
  • the esters may be chosen especially from fatty acid esters, for example: cetostearyl octanoate, isopropyl alcohol esters, such as isopropyl myristate or isopropyl palmitate, ethyl palmitate, 2-ethylhexyl palmitate, isopropyl stearate or isostearate, isostearyl isostearate, octyl stearate, hydroxylated esters, for instance isostearyl lactate, octyl hydroxystearate, diisopropyl adipate, heptanoates, and especially isostearyl heptanoate, alcohol or polyalcohol octanoates, decanoates or ricinoleates, for instance propylene glycol dioctanoate, cetyl octanoate, tridecyl octanoate, 2-ethylhexyl 4-dih
  • the volatile hydrocarbon-based oils may be chosen from hydrocarbon-based oils containing from 8 to 16 carbon atoms, and especially branched C 8 -C 16 alkanes (also known as isoparaffins), for instance isododecane (also known as 2,2,4,4,6- pentamethylheptane), isodecane, isohexadecane and, for example, the oils sold under the trade names Isopars ® or Permethyls ® .
  • the compositions according to the invention may also contain volatile or nonvolatile silicone oils.
  • the nonvolatile silicone oils that may be used in the composition according to the invention may be nonvolatile polydimethylsiloxanes (PDMS), polydimethylsiloxanes comprising alkyl or alkoxy groups that are pendent and/or at the end of a silicone chain, these groups each containing from 2 to 24 carbon atoms, phenyl silicones, for instance phenyl trimethicones, phenyl dimethicones, phenyl trimethylsiloxy diphenylsiloxanes, diphenyl dimethicones, diphenyl methyldiphenyl trisiloxanes and 2-phenylethyl trimethylsiloxysilicates, and dimethicones or phenyltrimethicones with a viscosity of less than or equal to 100 cSt, and mixtures thereof.
  • PDMS nonvolatile polydimethylsiloxanes
  • phenyl silicones for instance phenyl trimeth
  • Volatile silicone oils that may more particularly be used include volatile linear or cyclic silicone oils, especially those with a viscosity ⁇ 8 centistokes (8 x 10 "6 mVs) and especially containing from 2 to 10 silicon atoms and in particular from 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups containing from 1 to 10 carbon atoms.
  • volatile silicone oils that may be used in the invention, mention may be made especially of dimethicones with a viscosity of 5 and 6 cSt, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexa- siloxane, heptamethylhexyltrisiloxane, heptamethyloctyltrisiloxane, hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane and dodecamethylpentasiloxane, and mixtures thereof.
  • Volatile fluoro oils such as nonafluoromethoxybutane or perfluoro- methylcyclopentane, and mixtures thereof, may also be used.
  • compositions according to the invention may also advantageously comprise at least one compound chosen from waxes and pasty iatty substances, and mixtures thereof.
  • the wax is solid at room temperature (25°C), has a reversible solid/liquid change of state, has a melting point of greater than 30°C, which may be up to 200°C and a hardness of greater than 0.5 MPa, and has an anisotropic crystal organization in the solid state. It may be a hydrocarbon-based wax, fluoro wax and/or silicone wax and may be of animal, plant, mineral or synthetic origin.
  • compositions in accordance with the present invention comprise at least one wax chosen from waxes approved for food use.
  • a "wax approved for food use” covers ozokerite, rice wax, and the waxes referenced in the Codex alimentarius, more particularly including the waxes referenced in table 1 of the Codex alimentarius.
  • compositions in accordance with the present invention advantageously comprise a wax chosen from beeswax, ozokerite, rice wax, carnauba wax, candelilla wax and microcrystalline waxes, and mixtures thereof.
  • the wax compounds are food grade compounds as defined previously, and more particularly are referenced in the US code of Federal Regulation Title 21 Chap I Part 184.
  • the wax used in the cosmetic compositions in accordance with the invention is chosen from the microcrystalline wax sold by Paramelt and more particularly ozokerite, beeswax, candelilla wax or carnauba wax sold by Strahl & Pitsch, and mixtures thereof.
  • waxes are preferably used under a form specified by the supplier as being convenient for food industry.
  • the wax(es) approved for food use is or are present in the cosmetic compositions in accordance with the present invention in a content ranging from 1% to 50%, in particular from 3% to 40%, in particular from 5% to 30% and especially from 7% to 20% by weight relative to the total weight of the compositions.
  • compositions according to the invention may comprise one or more waxes chosen, for example, from synthetic waxes, for instance polyethylene wax (preferably with a molecular weight of between 400 and 600) or Fischer-Tropsch waxes, silicone waxes, for instance alkyl or alkoxy dimethicones containing from 16 to 45 carbon atoms, paraffin waxes, ceresins, for instance isoparaffins with a melting point of less than 40°C, such as EMW-0003, sold by the company Nippon Seirou, ⁇ -olefin oligomers, such as the polymers Performa V ® 825, 103 and 260, sold by the company New Phase Technologies; ethylene-propylene copolymers, such as Performalene ® EP 700, and mixtures thereof.
  • synthetic waxes for instance polyethylene wax (preferably with a molecular weight of between 400 and 600) or Fischer-Tropsch waxes, silicone waxes, for instance alkyl or alkoxy dimethicones
  • compositions in accordance with the present invention may also comprise at least one pasty compound.
  • pasty refers to a fatty compound with a reversible solid/liquid change of state and comprising, at a temperature of 25°C, a liquid fraction and a solid fraction.
  • the term pasty also means polyvinyl laurate. Polyol esters are most particularly suitable as pasty compounds according to the invention.
  • polyol esters that may be used in the context of the present invention are commercially available or may be prepared in a conventional manner. They are generally of plant origin and may be obtained especially by mono- or polyesterification of a polyol with a C 2 -C 34 monocarboxylic acid, for instance a fatty acid or with a dicarboxylic acid such as a diacid dimer.
  • the ester obtained may especially be a polyester, a triester, a diester, a monoester or a mixture thereof.
  • the ester may be a mixture of two or more types of ester formed with different carboxylic acids.
  • esters with a relatively high molecular weight, ranging from about 200 to 1300 g/mol, may be obtained.
  • a polyol dicarboxylate In the esterification reaction with a dicarboxylic acid, a polyol dicarboxylate may be obtained, which has a weight-average molecular weight, determined by gel permeation chromatography (GPC), ranging from 200 to 20 000 g/mol and preferably between 2000 and 4000 g/mol.
  • GPC gel permeation chromatography
  • polyol and “polyhydric alcohol” should be understood as meaning any organic molecule comprising at least two free hydroxyl groups.
  • the polyhydric alcohols that are advantageously suitable for the formulation of the cosmetic compositions according to the present invention are those especially containing from 2 to 20 carbon atoms, in particular from 3 to 10 carbon atoms and more particularly from 4 to 6 carbon atoms.
  • the polyol may be chosen, for example, from a diol dimer, glycerol, propylene glycol, butylene glycol, pentylene glycol, hexylene glycol, dipropylene glycol, diethylene glycol, sorbitol, hydroxypropyl sorbitol and 1,2,6-hexanetriol; glycol ethers (especially containing from 3 to 16 carbon atoms) such as mono-, di- or tripropylene glycol (Ci-C 4 )alkyl ethers and mono-, di- or triethylene glycol (Ci-C 4 )alkyl ethers; and mixtures thereof.
  • diol dimer i.e. saturated diols produced by hydrogenation of the corresponding diacid dimers.
  • a diol dimer may be produced by hydrogenation of a diacid dimer, which is itself obtained by dimerization of an unsaturated fatty acid especially of C 8 to C 34 , such as those mentioned previously, especially of C 12 to C22 and in particular of C 16 to C 20 , preferably C 18 such as, for example, oleic acid and linoleic acid.
  • the polyols that are more particularly suitable are sugars chosen from monosaccharides, disaccharides and trisaccharides. Illustrations of these sugars that may especially be mentioned include monosaccharides such as xylose, arabinose, galactose, fructose, mannose and glucose, and mixtures thereof. Illustrations of disaccharide polyols that may more particularly be mentioned include maltose, lactose and sucrose and combinations thereof.
  • the monocarboxylic acid that may be used in the present invention may contain from 2 to 34 carbon atoms and especially from 10 to 32 carbon atoms.
  • - saturated linear acids such as butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid, nonadecanoic acid, eicosanoic acid, docosanoic acid and tetracosanoic acid,
  • branched fatty acids for instance isobutanoic acid, isopentanoic acid, pivalic acid, isohexanoic acid, isoheptanoic acid, isooctanoic acid, dimethyloctanoic acid, isononanoic acid, isodecanoic acid, isoundecanoic acid, isododecanoic acid, isotridecanoic acid, isotetradecanoic acid, isopentadecanoic acid, isohexadecanoic acid, isoheptadecanoic acid, isooctadecanoic acid, isononadecanoic acid, isoeicosanoic acid, 2-ethylhexanoic acid, 2-butyloctanoic acid, 2-hexyldecanoic acid, 2-octyldodecanoic acid, 2-decyltetradecanoic acid, 2-dodecyl
  • - unsaturated linear C 8 to C 34 fatty acids such as undecenoic acid, linderic acid, myristoleic acid, palmitoleic acid, oleic acid, linoleic acid, elaidinic acid, gadolenoic acid, eicosapentaenoic acid, docosahexaenoic acid, erucic acid, brassidic acid and arachidonic acid,
  • - hydroxy acids such as 2-hydroxybutanoic acid, 2-hydropentanoic acid, 2-hydroxyhexanoic acid, 2-hydroxyheptanoic acid, 2-hydroxyoctanoic acid, 2-hydroxynonanoic acid, 2-hydroxydecanoic acid, 2-hydroxyundecanoic acid,
  • 2-hydroxydodecanoic acid 2-hydroxytridecanoic acid, 2-hydroxytetradecanoic acid, 2- hydroxyhexadecanoic acid, 2-hydroxyheptadecanoic acid, 2-hydroxyoctadecanoic acid, 12-hydroxyoctadecanoic acid, 2-hydroxynonadecanoic acid, 2-hydroxyeicosanoic acid, 2- hydroxydocosanoic acid and 2-hydroxytetracosanoic acid, - cyclic acids such as cyclohexanoic acid, hydrogenated rosin, rosin, abietic acid, hydrogenated abietic acid, benzoic acid, p-oxybenzoic acid, p-aminobenzoic acid, cinnamic acid, p-methoxycinnamic acid, salicylic acid, gallic acid, pyrrolidonecarboxylic acid and nicotinic acid, and
  • fatty acids of natural origin such as the fatty acids of orange oil, of avocado oil, of macadamia oil, of olive oil, of hydrogenated soybean oil, of jojoba oil, of palm oil, of castor oil, of wheatgerm oil, of saffron oil, of cottonseed oil and of mink oil, and mixtures thereof.
  • the dicarboxylic acid that may be used according to the invention should contain at least two carboxylic groups per molecule.
  • n is an integer from 1 to 16 and preferably from 3 to 16.
  • dicarboxylic acids that are suitable for the invention, mention may be made especially of malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, 1,9-nonamethylenedicar- boxylic acid, 1,10-decamethylenedicarboxylic acid, 1,11-undecamethylenedicarboxylic acid, lj ⁇ -dodecamethylenedicarboxylic acid, ljlS-tridecamethylenedicarboxylic acid, ljH-tetradecamethylenedicarboxylic acid, ljlS-pentadecamethylenedicarboxylic acid and ljl ⁇ -hexadecamethylenedicarboxylic acid, and mixtures thereof.
  • the dicarboxylic acid may also be a diacid dimer.
  • diacid dimer denotes a diacid obtained by polymerization reaction, especially by intermolecular dimerization of at least one unsaturated fatty acid especially of C 8 to C 34 , such as those mentioned previously, especially Of C 12 to C22 and in particular of C 16 to C 20 , preferably of
  • C 18 such as, for example, oleic acid and linoleic acid.
  • Polyol polyesters in which the fatty acid ester units of the polyester comprise saturated or unsaturated chain lengths chosen such that the compound has the required behavior in terms of pasty compounds according to the invention, are also most particularly suitable as polyol esters.
  • the unsaturated fatty acid chains are typically branched chains and more particularly contain from 12 to about 22 and more particularly from about 18 to 22 carbon atoms.
  • the unsaturated fatty acid chains more particularly considered are monounsaturated and/or diunsaturated C 18 fatty acids.
  • These long chains may be combined with shorter saturated fatty acid chains. They are generally linear and contain from 2 to about 12, preferably from 6 to about 12 and more particularly from 8 to 12 carbon atoms.
  • the degree of esterification of these fatty acid esters is such that about 60% of the hydroxyl functions of the polyols and more particularly about 85% or even 95% of the hydroxyl functions of the polyols are esterified.
  • unsaturated long-chain fatty acid ester units mention may be made more particularly of lauroleates, myristoleates, palmitoleates, oleates, elaidates, eructates, linoleates, linolenates, arachidonates, eicosapentaenoates and docosahexaenoates.
  • lauroleates myristoleates, palmitoleates, oleates, elaidates, eructates, linoleates, linolenates, arachidonates, eicosapentaenoates and docosahexaenoates.
  • monounsaturated and diunsaturated fatty acid chains are preferred.
  • long-chain unsaturated fatty acid ester units mention may be made more particularly of arachidate, behenate, linoserate and serotate esters.
  • the short-chain saturated fatty acid ester units may be more particularly acetate, caproate, caprylate, caprate and laurate.
  • solid polyol fatty acid polyesters that are most particularly suitable for the invention, mention may be made more particularly of raffinose octaesters in which the esterifying fatty acid parts are linoleate and behenate, maltose hectaesters in which the esterifying fatty acid parts are derived from sunflower seed oil fatty acid and from lignoserate, sucrose octaesters in which the esterifying fatty acid parts are behenate and oleate, and sucrose octaesters in which the esterifying fatty acid parts are laurates, linoleates and behenates.
  • Such solid fatty acid polyesters may be obtained according to methods already described for the preparation of the polyol polyesters. In this respect, reference may be made especially to documents US 5 306 516, US 5 306 515, US 5 305 514, US 4 797 300, US 3 963 699, US 4 518 772 and US 4 517 360.
  • the composition according to the invention comprises at least one ester of at least one carboxylic acid containing 1 to 7 carbon atoms and of a polyol containing at least 4 hydroxyl groups, the said ester having for example a molecular mass of less than 5 000 g/mol.
  • the ester preferably has a molecular mass of less than 2 000, more preferably less than 1 000, more preferably still less than 900 g/mol.
  • the molecular mass of the ester is preferably greater than 100 g/mol.
  • esters are particularly interesting for enhancing the wear of the compositions incorporating them.
  • the polyol according to the invention may be a monosaccharide, a polyhydroxyaldehyde (aldose) or polyhydroxyketone (ketose), which is cyclized or not.
  • the polyol is preferably a monosaccharide cyclized in hemiacetal form.
  • the polyol may also be a polyol derived from a monosaccharide, such as eythritol, xylitol or sorbitol.
  • aldoses mention may be made of D-ribose, D-xylose, L-arabinose, D- glucose (or alpha-D-glucopyranose when in cyclic hemiacetal form), D-mannose and D- galactose.
  • the polyol may be a monosaccharide or a polysaccharide containing from 1 to 10 monosaccharide units, preferably from 1 to 4, more preferably 1 ot 2 monosaccharide units.
  • the polyol is preferably selected from erythritol, xylitol, sorbitol, glucose and sucrose.
  • the polyol according to the invention is preferably a disaccharide.
  • disaccharides mention may be made of sucrose (alpha-D-glucopyranosyl-(l-3)-beta-D- fructofuranose), lactose (beta-D-galactopyranosyl-l(l-4)-beta-D-glucopyranose) and maltose (alpha-D-glucopyranosyl-(l -4)-beta-D-glucopyranose).
  • the polyol may be a polysaccharide composed of two or more identical monosaccharide units or at least two different monosaccharide units.
  • the ester according to the invention may be composed of a polyol substituted by at least two different monocarboxylic acids or by at least three different monocarboxylic acids.
  • the ester may be obtained by copolymerizing two esters according to the invention, in particular by copolymerizing i) a sucrose substituted by benzoyl groups and ii) a sucrose substituted by acetyl and/or isobutyryl groups.
  • the ester preferably contains no polar group, in particular no hydroxyl group.
  • the acid is added in an amount sufficient to react with all of the hydroxyl groups of the polyol.
  • the polar groups are, for example, ionic or non-ionic polar groups selected from -COOH; -OH; ethylene oxide; propylene oxide; -PO 4 ; -NHR; -NR 1 R 2 with R 1 and R 2 optionally forming a ring and each representing a linear or branched C 1 to C 20 alkyl or alkoxy radical.
  • the acid is preferably a monocarboxylic acid containing 1 to 7 carbon atoms, preferably 1 to 5 carbon atoms. It may be selected in particular from acetic, n-propanoic, isopropanoic, n-butanoic, isobutanoic, tert-butanoic, n-pentanoic and benzoic acids.
  • the ester may be obtained from at least two different monocarboxylic acids.
  • the acids is an unsubstituted linear or branched acid.
  • the acid is preferably selected from acetic acid, isobutyric acid and benzoic acid.
  • the ester has sucrose diacetate hexa(2- methylpropanoate) as a chemical name, and can bear the INCI name sucrose acetate isobutyrate.
  • fractionated hydrogenated triglycerides and especially those sold by SIO hydrogenated plant oils, hydrogenated palm oil, cocoa butter and, for example, those sold by Karlshamns, solid cottonseed oil, for example the oil sold by SIO, and sucrose acetate isobutyrate, for example the product sold by Eastman Chemical.
  • lanolines and lanoline derivatives for instance acetylated lanolines, oxypropylenated lanolines or isopropyl lanolate, and mixtures thereof.
  • the amount in lanoline(s) will be also adjusted for avoiding any undesirable effect in particular in term of smell as soon as these compounds are inclined to oxidize with time.
  • silicone compounds such as high molecular weight polydimethylsiloxanes (PDMS) and in particular those with pendent chains of the alkyl or alkoxy type containing from 8 to 24 carbon atoms, and a melting point of 20-55°C, for instance stearyl dimethicones, especially those sold by the company
  • PDMS high molecular weight polydimethylsiloxanes
  • pendent chains of the alkyl or alkoxy type containing from 8 to 24 carbon atoms and a melting point of 20-55°C, for instance stearyl dimethicones, especially those sold by the company
  • the solid substances may be chosen for their efficacy in texturing a liquid fatty phase.
  • the compounds that are suitable in this respect have a melting point of greater than or equal to 50°C, in particular greater than or equal to 55°C or even ranging from 55 to
  • compositions according to the invention contain at least one hydrocarbon-based plant oil like for example canola oil, caprylic/capric acid triglycerides and/or one of their mixtures and at least one ester of at least one carboxylic acid containing 1 to 7 carbon atoms and of a polyol containing at least 4 hydroxyl groups, in particular the sucrose diacetate hexa(2-methylpropanoate) and at least one hydrogenated vegetable oil.
  • hydrocarbon-based plant oil like for example canola oil, caprylic/capric acid triglycerides and/or one of their mixtures and at least one ester of at least one carboxylic acid containing 1 to 7 carbon atoms and of a polyol containing at least 4 hydroxyl groups, in particular the sucrose diacetate hexa(2-methylpropanoate) and at least one hydrogenated vegetable oil.
  • compositions according to the invention contain about 10 to 40% by weight of hydrocarbon-based plant oil(s) in particular non hydrogenated vegetable oil(s), - about 20 to 70% by weight of ester(s) of at least one carboxylic acid containing 1 to 7 carbon atoms and of a polyol containing at least 4 hydroxyl groups, and about to 10 to 40% by weight of hydrogenated vegetable oil(s)
  • compositions may further contain at least one compound selected among waxes, dyestuffs and fillers as described here above, like for example rice starch and mixtures thereof.
  • the composition packaged according to the invention may comprise at least one aqueous medium, constituting an aqueous phase, which can form the continuous phase of the composition.
  • the aqueous phase may consist exclusively of water.
  • It may also comprise a mixture of water and of water-miscible organic solvent (miscibility in water of greater than 50% by weight at 25°C), for instance lower monoalcohols containing from 1 to 5 carbon atoms, such as ethanol or isopropanol, glycols containing from 2 to 8 carbon atoms, such as propylene glycol, ethylene glycol,
  • 1,3-butylene glycol or dipropylene glycol 1,3-butylene glycol or dipropylene glycol, C 3 -C 4 ketones and C 2 -C 4 aldehydes.
  • the cosmetic composition that is suitable for use in the present invention may be in the form of a simple emulsion, a water-in-oil or oil- in-water emulsion, a multiple emulsion (water-oil-water or oil-water-oil) or an inverse emulsion, the use of which is well known to those skilled in the art.
  • the aqueous phase (water and optionally the water-miscible organic solvent) may be present in a content ranging from 0.1% to 50% by weight, especially ranging from 0.5% to 40% by weight, in particular from 1% to 25% by weight and in particular from 1% to 10% by weight relative to the total weight of the composition.
  • the composition according to the invention may be anhydrous.
  • anhydrous composition means a composition comprising less than 10% by weight of water relative to the total weight of the composition, especially less than 5%, in particular less than 2% and more particularly less than 1% by weight of water relative to the total weight of the composition.
  • an anhydrous composition according to the invention is free of water.
  • the cosmetic composition in accordance with the invention may advantageously incorporate one or more dyestuffs, especially such as pigments or pearls conventionally used in cosmetic compositions.
  • pigments should be understood as meaning white or colored, mineral or organic particles, which are insoluble in an aqueous solution and which are intended to color and/or opacify the corresponding cosmetic composition.
  • mineral pigments that may be used in the invention, mention may be made of zirconium oxide or cerium oxide and also zinc oxide or chromium oxide, ferric blue, manganese violet, ultramarine blue and chromium hydrate.
  • pearls should be understood as meaning iridescent or noniridescent colored particles of any form, produced especially by certain mo Husks in their shell or else synthesized, and which have a color effect by optical interference.
  • These dyestuffs may be present in a proportion of from 0.01% to 40% by weight, especially from 0.1% to 20% by weight and in particular from 0.5% to 15% by weight, or even from 1% to 10% by weight, relative to the total weight of the cosmetic composition.
  • the dyestuffs may be dyestuffs containing at least two materials, said dyestuff being referenced in the Codex alimentarius or consisting exclusively of materials referenced in the Codex alimentarius.
  • it is a dyestuff chosen from the compounds referenced in the
  • Codex alimentarius and pearls consisting of materials referenced in the Codex alimentarius, and mixtures thereof. Illustrations of these dyestuffs that may be mentioned more particularly include mineral pigments such as titanium oxides and iron oxides, water-soluble or liposoluble coloring agents, for instance Sudan red, ⁇ -carotene, beetroot juice, the disodium salt of ponceau, the disodium salt of alizarine green, quinoline yellow, DC Red No. 7, DC Green No. 6, DC Yellow No. 11, DC Violet No. 2, DC Orange No.
  • mineral pigments such as titanium oxides and iron oxides
  • water-soluble or liposoluble coloring agents for instance Sudan red, ⁇ -carotene, beetroot juice, the disodium salt of ponceau, the disodium salt of alizarine green, quinoline yellow, DC Red No. 7, DC Green No. 6, DC Yellow No. 11, DC Violet No. 2, DC Orange No.
  • pearls based on mica coated with titanium and/or with iron oxide pearls based on mica coated with titanium and/or with iron oxide and surface-coated with at least one organic dye, for instance carbon black, and pearls based on mica coated with aluminum, silver and/or gold and, where appropriate, surface-coated with at least one organic dye.
  • the base material and the abovementioned surface coatings are materials approved for food use.
  • TiO 2 is authorized under the reference E171, iron oxide under the reference E172, carbon black under the reference E153, aluminum under the reference E 174, and gold under the reference E 175.
  • Such composite materials are especially sold by the company Merck under the name Candurin ® .
  • lakes mention may be made more particularly of carbon black, pigments of the type such as organic barium, strontium, calcium, aluminum or titanium lakes, including those submitted for certification by the Food and Drug Administration (FDA) (for example FD & C), lakes based on cochineal carmine, or the diketopyrrolopyrroles (DPP) described in documents EP-A-542 669, EP-A-787 730, EP-A-787 731 and WO-A-96/08537.
  • FDA Food and Drug Administration
  • DPP diketopyrrolopyrroles
  • pigments of "lake" type that are most particularly suitable for the invention, mention may be made especially of those sold by LCW Sensient under the names FD&C Yellow No. 5/E102, FD&C Yellow No. 6/E110, FD&C Blue No. 1/E132, FD&C Red No. 40/E129, FD&C Blue No. 2 aluminum lake, FD&C Yellow No. 5 aluminum lake, FD&C Yellow No. 6 aluminum lake, FD&C Blue No. 1 aluminum lake, FD&C Red No. 40 aluminum lake and FD&C Green No. 3 aluminum lake.
  • FD&C Blue No. 1 aluminum lake, FD&C Green No. 3 aluminum lake, FD&C Yellow No. 5 aluminum lake, FD&C Yellow No. 6 aluminum lake and FD&C Red No. 40 aluminum lake are most particularly advantageous.
  • these dyestuffs are especially advantageous for affording an effect other than a simple conventional shade effect, i.e. a unified and stabilized effect as produced by standard dyestuffs, for instance monochromatic pigments.
  • the term "stabilized" means free of a color variability effect according to the angle of observation.
  • the effect obtained with the pearls and/or lakes may be an effect chosen from metallic effects, and especially a mirror, soft- focus and/or rainbow effect.
  • compositions may obviously comprise other organic or inorganic coloring substances.
  • D&C Orange No. 11 D&C Red No. 6, D&C Red No. 7, D&C Red No. 17, D&C Red
  • the organic dyestuff may comprise an organic lake supported on an organic support such as colophony or aluminum benzoate, for example.
  • organic lakes that may be mentioned in particular are those known under the following names: D&C Red No. 2 Aluminum lake, D&C Red No. 3 Aluminum lake, D&C Red No. 4 Aluminum lake, D&C Red No. 6 Aluminum lake, D&C Red No. 6
  • D&C Red No. 6 Potassium lake D&C Red No. 7 Aluminum lake, D&C Red No. 7 Barium lake, D&C Red No. 7 Calcium lake, D&C Red No. 7 Calcium/Strontium lake, D&C Red
  • Aluminum lake D&C Blue No. 1 Aluminum lake, D&C Green No. 3 Aluminum lake, D&C Orange No. 4 Aluminum lake, D&C Orange No. 5 Aluminum lake, D&C Orange No. 5 Zirconium lake, D&C Orange No. 10 Aluminum lake, D&C Orange No. 17 Barium lake, D&C Yellow No. 5 Aluminum lake, D&C Yellow No. 5 Zirconium lake, D&C Yellow No. 6 Aluminum lake, D&C Yellow No. 7 Zirconium lake, D&C Yellow No. 10 Aluminum lake.
  • compositions according to the invention may also contain diffracting agents, goniochromatic agents and/or reflective particles.
  • compositions according to the instant invention contain dyestuff considered as being food grade compound as described here- above.
  • dyestuff can be chosen from dyestuff having the specifications given in the US Code of Federal Regulation Title 21 Chap I parts 73, 74 and 82.
  • the dyestuff will in particular be made of at least 50% by weight, more particularly at least 75% by weight, especially 90% by weight of the total weight, of "food grade compounds" as defined here-above.
  • these compositions may be free of non food grade dyestuff.
  • the cosmetic compositions also generally contain fillers of mineral or organic origin.
  • Nonpigmentary inorganic compounds approved by the Codex alimentarius and more particularly referenced in table 1 thereof are most particularly suitable for the invention.
  • talc precipitated calcium carbonate, magnesium carbonate, rice starch and magnesium hydrogen carbonate.
  • compositions according to the invention may also comprise any ingredient conventionally used as additives in cosmetics and dermatology.
  • additives are advantageously chosen from the food additives proposed in table 1 of the Codex alimentarius, for example antioxidants, thickeners, sequestrants, acidifying or basifying agents and preserving agents, and mixtures thereof.
  • compositions according to the invention may also contain flavorings and/or fragrances.
  • the amounts of these various ingredients are those conventionally used in the fields under consideration and range, for example, from 0.01% to 20% by weight relative to the total weight of the composition.
  • the cosmetic compositions according to the invention may also have a gloss of greater than or equal to 5, in particular greater than or equal to 10, especially greater than or equal to 15, more particularly greater than or equal to 20, especially greater than or equal to 25, greater than or equal to 30, or even about 50.
  • gloss denotes the gloss as may be measured by the following method, using a gonioreflectometer machine, for instance the GRM-2000 machine (from
  • Micromodule using an azimuth illumination angle of 30° relative to the normal of the sample, a specular reflection (R) detection angle of -30° and a diffuse reflection (D) detection angle of 0° .
  • the foam support bearing the transparent adhesive plaster is then attached, by bonding by means of its adhesive face, to a metal plate 40x70 mm in size.
  • the assembly consisting of the support bonded to the metal plate forms a specimen.
  • the operator places the specimen on a hotplate set at a temperature of 38.5 °C, for example a hotplate of the type N81076 sold by the company Fisher Bioblock, and waits for the face of the support bearing the adhesive coating to reach a temperature of 33 ⁇ 1°C.
  • the operator manually applies a film about 15 ⁇ m thick of the cosmetic product to the Blenderm ® coating.
  • the cosmetic product which is, for example, a lipstick, was stored at 24 ⁇ 2°C.
  • the action performed by the operator to deposit the film of product consists of a to-and-fro motion, so as to obtain a uniform deposit.
  • the application of the product to the support is preferably performed so as to be as representative as possible of the real conditions of application of the product.
  • the same test product is applied in an identical manner to the five same specimens prepared previously.
  • the film of product is left to dry, the specimen being placed on the hotplate, such that the support remains at 33 ⁇ 1°C for 10 minutes.
  • the intensity of the specular reflection and that of the diffuse reflection of the film of product are measured at the incidences specified previously, for each of the five specimens.
  • the gloss Gloss t is calculated for each specimen via the ratio R/D for this specimen.
  • the weighting of the specular reflection measurement, generally used alone to characterize the gloss, by the diffuse reflection measurement (representative of the color/lightness of the sample) allows the visual perception of the gloss to be better appreciated.
  • the mean gloss value Gloss may finally be calculated:
  • compositions according to the invention may be suitable for forming a deposit with a wear of color index of greater than or equal to 30%, preferably greater than or equal to 40%, preferably greater than or equal to 45%, preferably greater than or equal to 50%, especially greater than or equal to 55%, in particular greater than or equal to 60%, or even greater than or equal to 65%, or greater than or equal to 70%.
  • the wear of color index of the deposit obtained with the composition according to the invention may be determined according to the measuring protocol described below.
  • a support (40 mm x 70 mm rectangle) consisting of an acrylic coating
  • the color L* o a* o b* o of the support, on the acrylic coating face, is measured using a Minolta CR 300 colorimeter.
  • the support thus prepared is preheated on a hotplate maintained at a temperature of 40°C in order for the surface of the support to be maintained at a temperature of 33°C ⁇ 1°C.
  • the hot support is removed from the plate and the composition is applied throughout the nonadhesive surface of the support (i.e. over the surface of the acrylic coating), spreading it out using a brush to obtain a deposit of about 15 ⁇ m of the composition.
  • the assembly is returned to the hotplate and left to dry for 10 minutes.
  • the support is then bonded via its adhesive face (adhesive face of the foam layer) to an anvil 20 mm in diameter equipped with a screw pitch.
  • a specimen of the support/deposit assembly is then cut out using a punch 18 mm in diameter.
  • the anvil is then screwed onto a press (Statif Manuel Imada SV-2 from the company Someco) equipped with a tensile testing machine (Imada DPS-20 from the company Someco).
  • a strip 33 mm wide and 29.7 cm long is drawn on a sheet of white photocopying paper with a basis weight of 80 g/m 2 , a first line is marked 2 cm from the edge of the sheet, and a second line is then marked 5 cm from the edge of the sheet, the first and second lines thus delimiting a box on the strip; next, a first mark and a second mark located in the strip at reference points 8 cm and 16 cm, respectively, from the second line, are applied. 20 ⁇ l of water are placed on the first mark and 10 ⁇ l of refined sunflower oil (sold by the company Lesieur) are placed on the second mark.
  • the white paper is placed on the base of the press and the specimen placed on the box of the strip of paper is then pressed at a pressure of about 300 g/cm exerted for 30 seconds. Before pressing again, the specimen is removed and a measurement corresponding to the transfer after pressure is taken. The specimen is then placed again just after the second mark (i.e. next to the box), a pressure of about 300 g/cm 2 is again exerted, and the paper is displaced, in a rectilinear manner as soon as the contact is made, at a speed of 1 cm/s over the entire length of the strip such that the specimen passes through the water and oil deposits.
  • the wear of color index of the composition is equal to the ratio:
  • the measurement is performed on 6 supports in succession and the transfer index corresponds to the mean of the 6 measurements obtained with the 6 supports.
  • the cosmetic compositions according to the invention may have a covering power of greater than or equal to 30, in particular greater than or equal to 50, especially greater than or equal to 60, more particularly greater than or equal to 80 and especially ranging from 90 to 100, or even of about 100.
  • This covering power may be measured via the following method.
  • the composition is blended beforehand so as to obtain a viscous paste.
  • the formulation is then spread to a thickness of 50 ⁇ m onto an Erichsen type 24/5 contrast card, with a black background and a white background, and the trichromatic coordinates (X, Y and Z) are measured using a CH-2002 or CR-3700 colorimeter.
  • the covering power is equal to 100 x Yb/Yw where Yb is the mean value of Y on the black background and Yw is the mean value of Y on the white background.
  • a covering power of 100 corresponds to a totally opaque formulation.
  • compositions according to the invention may be in the form of a colored or uncolored product or in the form of an antisun product. They may especially contain cosmetic active agents. They may then be used as a care or treatment base for the lips, for instance lip balms, for protecting the lips against the cold and/or sunlight and/or the wind.
  • cosmetic active agents that may be used in the invention, mention may be made of sunscreens, vitamins A, E, C and B3, provitamins, for instance D-panthenol, calmative active agents, for instance ⁇ -bisabolol, aloe vera or allantoin, plant extracts or essential oils, protective or restructuring agents, for instance ceramides, refreshing active agents, for instance menthol and derivatives thereof, emollients (cocoa butter), moisturizers (arginine PCA), anti-wrinkle active agents and essential fatty acids, and mixtures thereof.
  • the composition of the invention may also be in the form of a lip makeup product, for instance a lipstick or a lip gloss, optionally having care or treating properties.
  • the assembly according to the invention is in the form of a lipstick, in particular as illustrated by figure 7, or a lip gloss as represented in figure 5.
  • the compositions according to the invention may be obtained according to the preparation processes conventionally used in cosmetics or dermatology.
  • compositions packaged according to the invention may be in very varied forms.
  • they may be in the form of a solution, a paste or a cream.
  • They may be an emulsion, especially an oil-in-water or water-in-oil emulsion, a solid or soft anhydrous gel, or may be in the form of loose or compacted powder, cast as a stick or a dish, and even in two-phase form.
  • a composition more particularly intended to be applied to the skin, especially of the face, the choice of a packaging of the type illustrated by figures 1, 3 and 4 is preferred.
  • a device such as that shown in figure 2 is found to be most particularly suitable.
  • a device such as that shown in figure 6 is, on the other hand, more particularly suitable for fluid compositions intended to be applied to keratin fibers and more particularly the eyelashes.
  • the makeup assembly according to the invention is chosen so as to be adapted to the galenical form of the composition.
  • composition in solid form i.e. in hard form (which does not flow under its own weight), especially cast or compacted, for example as a stick or a dish.
  • a composition in accordance with the invention may also be in the form of a "liquid gloss".
  • liquid gloss and similarly the terms “liquid lipstick” and “lip gloss” denote a fluid product intended to be applied to the lips.
  • the makeup assembly according to the invention may be as illustrated in figure 5.
  • the assembly is suitable for the packaging of a composition of cast type for use as a foundation, an eyeshadow or a makeup rouge.
  • Such an assembly may be in accordance with that illustrated in figure 1.
  • figure 1 schematically shows, in perspective, an example of a packaging assembly according to the invention
  • figure 2 is a schematic view in perspective of another example of a packaging assembly according to the invention
  • figure 3 is a schematic view in longitudinal cross section of another example of a packaging assembly in accordance with the invention
  • figure 4 is also a schematic view in longitudinal cross section of another example of a packaging assembly in accordance with the invention
  • - figure 5 also shows a schematic view in longitudinal cross section of another example of a packaging assembly more particularly intended for the application of a fluid composition
  • figure 6 is a schematic view in longitudinal cross section of another example of a packaging assembly also more particularly intended for applying a fluid composition
  • figure 7 shows a schematic view in perspective of another packaging assembly more particularly intended for applying a composition of solid type.
  • Figure 1 shows a packaging assembly 1 more particularly intended for a solid or compacted composition C.
  • the packaging assembly comprises a case 11 consisting of a base body 12 and a lid 11 articulated thereon.
  • the base body 12 comprises a compartment 13 housing the composition, consisting in the illustrated example of a foundation in pasty form.
  • the base body comprises a housing for receiving a support 14 intended for applying the composition.
  • the assembly 20 is more particularly suitable for packaging a composition of nail varnish type.
  • the composition C is contained in a container 22 closed by a cap 23.
  • This cap supports a cosmetic applicator 24 comprising an application unit consisting of a brush for applying the varnish to the nails.
  • Figure 3 is a partial schematic longitudinal cross section of another example of a packaging and application assembly 30 in accordance with the invention.
  • the container 31 comprises a neck 32 on which is mounted a component 33 for supporting a porous application unit 34, for example a foam.
  • a protective cover 35 can be screwed onto the support component 33.
  • the application member 34 is, for example, an open-cell foam.
  • the product C is, for example, a foundation or a care product.
  • Figure 4 shows another type of packaging assembly in accordance with the invention.
  • the applicator 41 is loaded with composition C through a perforated wall 42 separating a housing 43 receiving the application member when the applicator closes the container and a space 44 containing the reserve of product 45.
  • the applicator is, for example, fixed onto the container 46 by screwing.
  • Figure 5 shows an example of a packaging assembly 5 more particularly intended for applying a fluid composition to the lips.
  • the container contains the fluid composition to be applied to the lips C. It is combined with an applicator 52 comprising an application unit 53 mounted at the end of a stem 54 connected to a handle unit 55 which also constitutes a cap for closing the container 51.
  • the container 51 is equipped with a unit 56 for draining the stem 54 and the application unit 53 in a conventional manner.
  • Figure 6 shows a packaging and application assembly 60 suitable for application to the eyelashes.
  • a container 61 containing a composition C to be applied, for example a water-based or anhydrous mascara, and an applicator 62 and, at the other end, a handle unit 67 also constituting a cap for closing the container 61.
  • This container comprises a neck 68 onto which the closing cap 67 may be fixed and in which is housed a draining unit 69 for wiping the stem 63 and the application unit 64, when the applicator is removed from the container 61.
  • the application unit 64 is, in the example under consideration, a brush that may comprise a twisted metal core, between the turns of which the bristles are trapped.
  • the application unit 64 may also be a comb.
  • Figure 7 shows another example of a conditioning assembly according to the invention 70 comprising a composition C consisting in this example of a stick of lipstick whose composition may be as defined in examples 1 to 12 below.
  • the stick of composition is supported by a holding unit 71 and may be housed, when not in use, in a compartment 72.
  • This assembly also comprises a cap 73 for sealing off the container containing the composition and in which the outer end of the stick may be housed when not in use.
  • the compounds can be independently one from the other be chosen from compounds approved for food use. According to one embodiment they can independently advantageously be food grade compounds as defined before in the application.
  • the following compounds can be used in the examples: the caprylic/capric acid triglycerides sold by Stepan under the trademark NEOBEE M-5, the sucrose acetate isobutyrate sold by Eastman under the trademark Eastman SAIB-100, the deodorized apricot kernel oil sold by Nestle under the trademark Apricot Kernel Oil Type C, - the microcrystalline wax sold by Paramelt under the trademark Micro Wax
  • the waxes, the pasty compounds and the oils are melted at 100°C.
  • the ground pigmentary material containing the iron oxides and/or the aluminum lakes is incorporated therein and the mixture is then stirred for 45 minutes. At the end of the stirring period, the pearls and optionally the flavoring are added.
  • the mixture is poured into a lipstick mold preheated to 42°C. The mold is then placed in a refrigerator until the temperature of the mold reaches 2°C. The sticks are then removed from the molds and the products are stored at 20°C for 24 hours.
  • composition is as follows: weight %
  • composition is as follows: weight %
  • composition is as follows: weight %
  • composition is as follows: weight %
  • composition is as follows: weight %
  • composition is as follows: weight % canola oil 19.32
  • Titanium dioxide 1.82
  • Table 1 below presents seven lipstick formulations incorporating, as dyestuffs, lakes and pearls approved for food use. These dyestuffs are specifically made to match the needs of the food industry. They consist only of an edible silicate of natural origin in combination with the widely approved food colorants titanium dioxide and/or iron oxide.
  • composition of the white substance used in combination with the various mixtures of pearls and lakes is as follows: weight %
  • Cast foundation formulation weight %

Abstract

La présente invention concerne un ensemble destiné au soin et/ou au maquillage de matière(s) kératinique(s), comprenant au moins : - un contenant délimitant au moins un compartiment - des moyens d'application associés au contenant, ainsi qu'une composition, placée à l'intérieur dudit compartiment, la composition comprenant au moins une phase grasse et étant constituée d'au moins 50 % en poids de composé(s) approuvé(s) pour un usage alimentaire relativement à son poids total.
PCT/IB2006/052392 2005-07-13 2006-07-13 Ensemble de maquillage et/ou de soin cosmetique WO2007007288A2 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR0552204 2005-07-13
FR0552204A FR2888475B1 (fr) 2005-07-13 2005-07-13 Ensemble de maquillage et/ou de soin cosmetique
US71212405P 2005-08-30 2005-08-30
US60/712,124 2005-08-30

Publications (2)

Publication Number Publication Date
WO2007007288A2 true WO2007007288A2 (fr) 2007-01-18
WO2007007288A3 WO2007007288A3 (fr) 2007-03-29

Family

ID=37478895

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2006/052392 WO2007007288A2 (fr) 2005-07-13 2006-07-13 Ensemble de maquillage et/ou de soin cosmetique

Country Status (1)

Country Link
WO (1) WO2007007288A2 (fr)

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8440237B2 (en) 2009-04-27 2013-05-14 Mary Kay Inc. Botanical anti-acne formulations
CN103110561A (zh) * 2012-12-14 2013-05-22 吴江市德佐日用化学品有限公司 一种防过敏唇膏
EP2509461A4 (fr) * 2009-12-07 2014-03-05 Kind Group Baume pour les lèvres doté d'une surface sphérique et son procédé de fabrication
WO2013108029A3 (fr) * 2012-01-20 2014-12-18 Cosmetic Warriors Limited Composition cosmétique liquide ou semi-solide
US9138401B2 (en) 2011-12-19 2015-09-22 Mary Kay Inc. Combination of plant extracts to improve skin tone
US10039366B1 (en) 2014-09-25 2018-08-07 Snugz/Usa Incorporated Dual balm applicator and method of manufacture
USD829996S1 (en) 2017-02-08 2018-10-02 Eos Products, Llc Lip product container
USD831891S1 (en) 2016-08-09 2018-10-23 Eos Products, Llc Lip product container
USD841252S1 (en) 2016-09-14 2019-02-19 Eos Products, Llc Lip product container
USD846808S1 (en) 2016-08-09 2019-04-23 Eos Products, Llc Lip product container
USD858891S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD858889S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD858888S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD858890S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD868380S1 (en) 2016-09-14 2019-11-26 Eos Products, Llc Lip product container
US10500152B2 (en) 2014-03-10 2019-12-10 Mary Kay Inc. Skin lightening compositions
USD940960S1 (en) 2016-08-09 2022-01-11 Eos Products, Llc Lip product container
USD968711S1 (en) 2016-09-14 2022-11-01 Eos Products, Llc Lip product container

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USD825860S1 (en) 2017-02-08 2018-08-14 Eos Products, Llc Lip product container
USD825856S1 (en) 2016-08-09 2018-08-14 Eos Products, Llc Lip product container
USD827935S1 (en) 2016-08-09 2018-09-04 Eos Products, Llc Lip product container
USD825861S1 (en) 2017-02-08 2018-08-14 Eos Products, Llc Lip product container
USD827205S1 (en) 2017-02-08 2018-08-28 Eos Products, Llc Lip product container
USD825858S1 (en) 2017-02-08 2018-08-14 Eos Products, Llc Lip product container
USD825859S1 (en) 2017-02-08 2018-08-14 Eos Products, Llc Lip product container
USD830638S1 (en) 2016-08-09 2018-10-09 Eos Products, Llc Lip product container
USD825857S1 (en) 2016-08-09 2018-08-14 Eos Products, Llc Lip product container

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3189231A (en) * 1963-01-16 1965-06-15 Fmc Corp Aerosol dispenser with sponge follower and method of making same
US5011855A (en) * 1982-04-16 1991-04-30 Nestec S.A. Cosmetic and dermatological compositions containing γ-linolenic acid
US5839616A (en) * 1997-08-14 1998-11-24 The Procter & Gamble Company Blow molded container having pivotal connector for an actuation lever
ES2151456A1 (es) * 1999-05-12 2000-12-16 Monasterio Cisterciense De Tul Procedimiento de obtencion de un producto cosmetico y producto obtenido con este procedimiento.

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3189231A (en) * 1963-01-16 1965-06-15 Fmc Corp Aerosol dispenser with sponge follower and method of making same
US5011855A (en) * 1982-04-16 1991-04-30 Nestec S.A. Cosmetic and dermatological compositions containing γ-linolenic acid
US5839616A (en) * 1997-08-14 1998-11-24 The Procter & Gamble Company Blow molded container having pivotal connector for an actuation lever
ES2151456A1 (es) * 1999-05-12 2000-12-16 Monasterio Cisterciense De Tul Procedimiento de obtencion de un producto cosmetico y producto obtenido con este procedimiento.

Cited By (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10682381B2 (en) 2009-04-27 2020-06-16 Mary Kay Inc. Botanical formulations
US8747926B2 (en) 2009-04-27 2014-06-10 Mary Kay Inc. Botanical formulations
US8481090B2 (en) 2009-04-27 2013-07-09 Mary Kay Inc. Botanical formulations
US11638735B2 (en) 2009-04-27 2023-05-02 Mary Kay Inc. Botanical formulations
US10953058B2 (en) 2009-04-27 2021-03-23 Mary Kay Inc. Botanical formulations
US9561198B2 (en) 2009-04-27 2017-02-07 Mary Kay Inc. Botanical formulations
US8440237B2 (en) 2009-04-27 2013-05-14 Mary Kay Inc. Botanical anti-acne formulations
EP2509461A4 (fr) * 2009-12-07 2014-03-05 Kind Group Baume pour les lèvres doté d'une surface sphérique et son procédé de fabrication
US10278477B2 (en) 2009-12-07 2019-05-07 Eos Products, Llc Lip balm with spherical surface and method for producing
US11337507B2 (en) 2009-12-07 2022-05-24 Eos Products, Llc Lip balm with spherical surface and method for producing
US10925376B2 (en) 2009-12-07 2021-02-23 Eos Products, Llc Lip balm with spherical surface and method for producing
US9585458B2 (en) 2009-12-07 2017-03-07 Eos Products, Llc Lip balm with spherical surface and method for producing
EP3066952A1 (fr) * 2009-12-07 2016-09-14 Eos Products S.A.R.L. Baume pour les lèvres doté d'une surface sphérique et son procédé de fabrication
US10780041B2 (en) 2011-12-19 2020-09-22 Mary Kay Inc. Combination of plant extracts to improve skin tone
US9138401B2 (en) 2011-12-19 2015-09-22 Mary Kay Inc. Combination of plant extracts to improve skin tone
US11865202B2 (en) 2011-12-19 2024-01-09 Mary Kay Inc. Combination of plant extracts to improve skin tone
US9861573B2 (en) 2011-12-19 2018-01-09 Mary Kay Inc. Combination of plant extracts to improve skin tone
WO2013108029A3 (fr) * 2012-01-20 2014-12-18 Cosmetic Warriors Limited Composition cosmétique liquide ou semi-solide
CN103110561A (zh) * 2012-12-14 2013-05-22 吴江市德佐日用化学品有限公司 一种防过敏唇膏
US10500152B2 (en) 2014-03-10 2019-12-10 Mary Kay Inc. Skin lightening compositions
US10039366B1 (en) 2014-09-25 2018-08-07 Snugz/Usa Incorporated Dual balm applicator and method of manufacture
USD846808S1 (en) 2016-08-09 2019-04-23 Eos Products, Llc Lip product container
USD940960S1 (en) 2016-08-09 2022-01-11 Eos Products, Llc Lip product container
USD870973S1 (en) 2016-08-09 2019-12-24 Eos Products, Llc Lip product container
USD831891S1 (en) 2016-08-09 2018-10-23 Eos Products, Llc Lip product container
USD868380S1 (en) 2016-09-14 2019-11-26 Eos Products, Llc Lip product container
USD858889S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD858891S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD841252S1 (en) 2016-09-14 2019-02-19 Eos Products, Llc Lip product container
USD968711S1 (en) 2016-09-14 2022-11-01 Eos Products, Llc Lip product container
USD858890S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD995917S1 (en) 2016-09-14 2023-08-15 Eos Products, Llc Lip product container
USD858888S1 (en) 2016-09-14 2019-09-03 Eos Products, Llc Lip product container
USD829996S1 (en) 2017-02-08 2018-10-02 Eos Products, Llc Lip product container

Also Published As

Publication number Publication date
WO2007007288A3 (fr) 2007-03-29

Similar Documents

Publication Publication Date Title
WO2007007288A2 (fr) Ensemble de maquillage et/ou de soin cosmetique
EP1901811A1 (fr) Traitement cosmetique de maquillage et/ou de soins
JP3466138B2 (ja) ポリアミド末端エステルでゲル化した液状脂肪相を含有する組成物
ES2285999T3 (es) Composicion cosmetica que comprende un ester de acido graso hidroxilado.
JP2006028181A (ja) シリコーンポリマーを含む２段コート式化粧用製品
JP2007023036A (ja) 二度塗り化粧品、その使用およびこの製品を含むメイクアップキット
WO2015014789A1 (fr) Composition cosmétique anhydre comprenant de l'alkylcellulose, au moins un ester de dextrine ramifié et au moins un alcool gras
FR2947175A1 (fr) Composition cosmetique comprenant un copolymere styrene/acrylate et une resine siliconee
EP1901706A2 (fr) Traitement cosmetique pour maquillage et/ou soin
WO2007007287A2 (fr) Procede de maquillage et/ou de soin cosmetique
ES2321938T3 (es) Composicion cosmetica de cuidado y maquillaje de las materias queratinicas que contiene un poliester.
WO2007007292A2 (fr) Produit cosmetique de maquillage et/ou de soin
JP2008133280A (ja) 少なくとも一つの揮発性炭酸エステルを含む化粧品組成物
JP5996155B2 (ja) 少なくとも一つの揮発性エステルを含む化粧品組成物
US20090123403A1 (en) Cosmetic Composition With Color And/Or Optical Effects
WO2007007290A1 (fr) Maquillage et/ou procede de soins
WO2007007293A2 (fr) Compositions cosmetiques en batonnet
JP2005336189A (ja) 化粧リップメイクアップまたはリップケア組成物
JP5068948B2 (ja) アルコキシル化アルコールエステルおよび炭化水素系エステル油を含む化粧品組成物
WO2007007294A2 (fr) Film de produit cosmetique
JP2006131636A (ja) オルガノゲルを形成できる無水の化粧料組成物
FR2943245A1 (fr) Composition cosmetique comprenant une cire diester et une huile siliconee phenylee
FR2888498A1 (fr) Composition cosmetique de type stick
WO2007007295A2 (fr) Dispositif d'emballage et de distribution d'une composition cosmétique
FR2888476A1 (fr) Dispositif de conditionnement et de distribution d'une composition cosmetique

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application
NENP Non-entry into the national phase in:

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

122 Ep: pct application non-entry in european phase

Ref document number: 06780074

Country of ref document: EP

Kind code of ref document: A2