CN115297834A - Eyeliner cosmetic - Google Patents

Eyeliner cosmetic Download PDF

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Publication number
CN115297834A
CN115297834A CN202180025766.3A CN202180025766A CN115297834A CN 115297834 A CN115297834 A CN 115297834A CN 202180025766 A CN202180025766 A CN 202180025766A CN 115297834 A CN115297834 A CN 115297834A
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CN
China
Prior art keywords
component
eyeliner
cosmetic
film
powder
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Pending
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CN202180025766.3A
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Chinese (zh)
Inventor
郡司理纱子
森洋辅
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Kose Corp
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Kose Corp
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Publication of CN115297834A publication Critical patent/CN115297834A/en
Pending legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/20Halogens; Compounds thereof
    • A61K8/21Fluorides; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/31Hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • A61Q1/10Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara

Abstract

The invention aims to develop an eyeliner cosmetic which not only has excellent long-lasting makeup, but also is easy to be removed by hot water when the cosmetic is removed, and has excellent flexibility, film forming property and non-dizzy property when being applied. The eyeliner cosmetic of the present invention for solving the problem is characterized by containing the following components (A) to (D): the water-based dispersion liquid for the water-based paint comprises (A) an alkyl acrylate/vinyl acetate copolymer dispersion (A-2) using a nonaqueous solvent (A-1) as a dispersion medium, (B) a dextrin fatty acid ester, (C) a hydrophobized surface-treated powder, and (D) a volatile oil agent.

Description

Eyeliner cosmetic
Technical Field
The present invention relates to an eyeliner cosmetic.
Background
The eyeliner is a cosmetic that emphasizes the eyes by drawing lines on the outlines of the eyes to make them look large. From the viewpoint of the method of using the cosmetic film to draw the contour of the eye, it is required to have a soft cosmetic film which is easy to draw a line smoothly without causing halation, has a film-forming property to form a dried film instantaneously, has a makeup-sustaining property to cope with bleeding caused by tear or sebum, and does not cause cracks due to continuous movement of the eyelid. In addition, since the contour of the eye is a very sensitive part, it is also important to simply remove the cosmetic film without strong wiping (ease of removal).
The eyeliner cosmetic is of an oil type or a water type. Here, the oil type means a nonaqueous or W/O type eyeliner cosmetic, and the water type means O/W or eyeliner composed of only water-soluble components. In general, the oil type is excellent in long-lasting makeup, and the water type is excellent in removability in hot water. For both oil-based types and water-based types, techniques for further improving the quality while taking advantage of the respective advantages have been developed. For example, a technique for obtaining a makeup cosmetic characterized by containing a nonaqueous polymer dispersion in which a polymer is dispersed in a volatile silicone can provide a makeup-sustaining effect that does not cause makeup due to sweat, tears, sebum, or the like (see patent document 1). There is also a technique of using a makeup cosmetic containing a core-shell polymer emulsion, a hydratable oil agent, and a microcrystalline wax, wherein the mass ratio of the hydratable oil agent to the microcrystalline wax is 1 to 1. Further, an eye cosmetic composition has been developed which contains a silicone film agent in an amount of 10.01 to 30 mass% and a volatile oil in an amount of 25 to 70 mass% based on the total amount of the eye cosmetic composition, and has excellent makeup retention properties with the volatile silicone oil in an amount of 25 mass% or more based on the total amount of the volatile oil and has a hardness of 30 or more and 100 or less (see patent document 3).
Documents of the prior art
Patent document
Patent document 1: japanese patent laid-open publication No. 10-087435,
patent document 2: japanese patent laid-open publication No. 2010-265225,
patent document 3: japanese patent laid-open publication No. 2017-218413.
Disclosure of Invention
Problems to be solved by the invention
The present invention addresses the problem of developing an eyeliner cosmetic that not only has excellent long-lasting makeup properties, but also is easily removed with hot water when the cosmetic is removed, and has an outer film that has excellent flexibility, film-forming properties, and non-iridescence when applied.
Means for solving the problems
The present inventors have conducted extensive studies and as a result, have developed an eyeliner cosmetic which comprises a combination of an alkyl acrylate/vinyl acetate copolymer dispersion with a dextrin fatty acid ester, a hydrophobized surface-treated powder, and a volatile oil agent, not only has excellent long-lasting property, but also can be easily removed by hot water, and the coating film has excellent flexibility, film forming property and non-staining property when being applied.
That is, the present invention relates to an eyeliner cosmetic composition, which comprises the following components (a) to (D):
(A) (A-2) an alkyl acrylate/vinyl acetate copolymer dispersion using (A-1) a nonaqueous solvent as a dispersion medium,
(B) Dextrin fatty acid ester,
(C) A hydrophobized surface-treated powder,
(D) A volatile oil agent.
ADVANTAGEOUS EFFECTS OF INVENTION
The present invention provides an eyeliner cosmetic which is excellent not only in long-lasting makeup but also in removability with hot water when removing the cosmetic, and is also excellent in film flexibility, film formability, and non-halation properties when applied.
Detailed Description
The present invention will be described in detail below. In the present specification, "-" means a range including numerical values before and after the range, and "%" means mass% when not particularly described. The "average particle diameter" in the present invention is a median particle diameter D50 value obtained by measurement using an image analyzer (LUZEX AP, manufactured by NIRECO corporation). In the case of the asymmetric shape, the median diameter D50 obtained from the distribution of the maximum particle diameter is defined as the average particle diameter in the present invention.
The component (A) used in the present invention is a dispersion in which an alkyl acrylate/vinyl acetate copolymer (A-2) is dispersed in a nonaqueous solvent (A-1).
The alkyl acrylate/vinyl acetate COPOLYMER (A-2) corresponds to the component recorded under the INCI name (International Nomenclature Cosmetic raw material labeling names) as ACRYLATES/VA COPOLYMER. The component (A) is obtained by copolymerizing alkyl (meth) acrylate with vinyl acetate, and 1 or 2 or more kinds of alkyl (meth) acrylate having an alkyl group of 1~4, 8 or 12 carbon atoms can be used as the alkyl (meth) acrylate. The mass ratio of the alkyl (meth) acrylate to vinyl acetate constituting the component (a) is not particularly limited, and is preferably in the range of 30 to 95 ((alkyl (meth) acrylate: vinyl acetate), more preferably in the range of 40 to 70. Within this range, the cosmetic properties, removability in hot water, flexibility of the film, film formability, and non-tingling properties when using a pen-type application are more preferable.
The number average molecular weight of the component (a-2) is not particularly limited, but is preferably 5 to 50 ten thousand, and more preferably 5 to 30 ten thousand, from the viewpoint of long-lasting makeup. The number average molecular weight is a polystyrene equivalent value obtained by gel permeation chromatography. The lower limit of the Tg of the polymer obtained by polymerizing only the alkyl (meth) acrylate among the monomers constituting the component (a) is preferably 10 ℃ or higher, more preferably 15 ℃ or higher, and still more preferably 20 ℃ or higher, from the viewpoint of easy removability in hot water. The upper limit is preferably 50 ℃ or lower, and more preferably 40 ℃ or lower.
The nonaqueous solvent (a-1) as the dispersion medium of the component (a) contains an organic solvent, a silicone-based solvent, and the like which can be blended into a cosmetic, and among them, in view of film forming property and non-blooming property when using a pen-type application, a volatile hydrocarbon oil, a fatty acid ester, a fatty acid, a silicone oil, and the like are preferable, and a volatile hydrocarbon oil is more preferable. The volatile hydrocarbon oil is a hydrocarbon having a boiling point at normal pressure of 260 ℃ or lower, and examples thereof include hydrocarbons having a side chain such as isooctane, isododecane, isohexadecane, and isoeicosene, isoparaffins, and mixtures thereof, which are obtained by polymerizing or copolymerizing isobutene, n-butene, or the like (the polymerization degree is preferably 4~6) and then hydrogenating the resulting product, and 1 or 2 or more kinds of these may be used in combination as needed. Of these, isododecane is preferred.
The fatty acid ester is not particularly limited, and the alkyl group of the constituent fatty acid is preferably 2 to 18, more preferably 4 to 16, and particularly preferably 8 to 12, from the viewpoint of preventing blushing when a pen-type coating is used. As preferable fatty acid esters, there can be exemplified, for example, neopentyl glycol di (2-ethylhexanoate), diethylhexyl succinate, ethylhexyl palmitate, isopropyl myristate, dilinoleic acid hydrogenated rosinate, tricaprylin (caprylic/capric) triglyceride, cetyl 2-ethylhexanoate, neopentyl glycol dicaprate, propylene glycol dicaprate, isotridecyl isononanoate, tris (2-ethylhexanoate), diisostearyl malate, 2-ethylhexyl p-methoxycinnamate, ethylhexyl salicylate, pentaerythritol tetrakis (2-ethylhexanoate), polyglyceryl-10 deca (ethylhexanoate), ethylhexyl hydroxystearate, tridecyl trimellitate, dipentaerythritol hexaisononanoate, diglycerol triisostearate and the like, and 1 or 2 or more of them can be used. Among them, neopentyl glycol di (2-ethylhexanoate), diethylhexyl succinate, ethylhexyl palmitate, isopropyl myristate, dilinoleoyl hydrocinnamate, tricaprylin, cetyl 2-ethylhexanoate, neopentyl glycol dicaprate, propylene glycol dicaprate, isotridecyl isononanoate, tri (2-ethylhexanoate), diisostearyl malate, 2-ethylhexyl p-methoxycinnamate, ethylhexyl salicylate are more preferable.
As the fatty acid, isostearic acid, stearic acid, oleic acid, lauric acid, palmitic acid, and the like can be exemplified. Examples of the silicone oil include volatile silicone oils such as diphenylsiloxyphenyltrimethicones, diphenylpolydimethylsiloxanes, octamethylcyclotetrasiloxane, dodecamethylcyclohexasiloxanes, methyltrimethylsiloxanes, octyltrimethicones, dimethylpolysiloxanes, decamethylcyclopentasiloxanes, and decamethyltetrasiloxane.
In the component (A), the alkyl acrylate/vinyl acetate copolymer (A-2) is contained as resin particles dispersed in the nonaqueous solvent (A-1). The average particle diameter is preferably 0.1 to 2 μm from the viewpoints of long-wearing property, easy removability in hot water, flexibility of a film, and freedom from bleeding when a pen-type paint is used. The average particle diameter of the resin particles was determined by the following method using a laser diffraction method. Using a Pasteur pipette, 5mL of component (A) was collected in a square glass cuvette having a length of 5mm, a width of 65mm and a height of 80mm, and mounted on a laser diffraction/scattering particle size distribution measuring apparatus [ LA-910A manufactured by horiba, ltd.). The concentration of the component (a) is adjusted so that the transmittance of the laser beam (red) is 80% to 90%, and then the result of measurement at a measurement temperature of 25 ℃ ± 1 ℃ is subjected to computer processing to determine the average particle diameter of the resin particles in the non-aqueous dispersion, and the value of the volume average (D50) is defined as the average particle diameter.
The component (a) can be obtained by a known method, for example, a method of polymerizing an alkyl (meth) acrylate and vinyl acetate in a nonaqueous solvent, or a method of dispersing the prepared alkyl acrylate/vinyl acetate copolymer in a nonaqueous solvent. From the viewpoint of film formability and non-halation when a pen type paint is used, the content mass ratio ((a-2)/(a-1)) of the nonaqueous solvent (a-1) to the alkyl acrylate/vinyl acetate copolymer (a-2) in the component (a) is preferably 1 or less. Examples of commercially available products of the component (A) include Nissetsu U-3712A (manufactured by Nippon Carbide Industry Co., ltd.) and the like, and the number average molecular weight and the average particle diameter of the alkyl acrylate/vinyl acetate copolymer (A-2) contained therein are within the above-mentioned ranges.
The content of the component (a-2) in the eyeliner cosmetic of the present invention is not particularly limited, and the lower limit is preferably 0.8% or more, more preferably 1% or more, further preferably 2% or more, and particularly preferably 3% or more. The upper limit is preferably 20% or less, more preferably 15% or less, still more preferably 10% or less, particularly preferably 8% or less, and most preferably 6% or less. Within this range, the cosmetic properties, removability in hot water, flexibility of the film, and film formability are more preferable.
The component (B) in the present invention is an ester of a fatty acid and dextrin. The dextrin fatty acid ester of the present invention may be any dextrin fatty acid ester as long as it is a substance that can be generally used in cosmetics. For example, the fatty acid used in the dextrin fatty acid ester of the present invention is not particularly limited, and the lower limit of the number of carbon atoms of the fatty acid is preferably 12 or more, more preferably 14 or more, and further preferably 16 or more, from the viewpoint of film formability and flexibility of the film. The upper limit value is preferably 22 or less, more preferably 20 or less, and still more preferably 18 or less. Specific examples of such fatty acids include ethylhexanoic acid, octanoic acid, decanoic acid, lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid, and behenic acid. The fatty acid used in the dextrin fatty acid ester may be either a linear or branched fatty acid, and is preferably a linear fatty acid from the viewpoint of film-forming properties; saturated and unsaturated fatty acids can be used, and saturated fatty acids are preferable from the viewpoint of film-forming properties. The substitution degree of the dextrin hydroxyl group with the fatty acid is not particularly limited, and the lower limit value is preferably 1 or more, and more preferably 1.7 or more. The upper limit value is preferably 3 or less, and more preferably 2.5 or less.
Examples of the component (B) include dextrin laurate, dextrin myristate, dextrin palmitate, dextrin (palmitic acid/ethylhexanoate), dextrin stearate, dextrin isostearate, dextrin behenate, and dextrin coco fatty acid ester. Among them, 1 or 2 or more selected from dextrin myristate, dextrin palmitate, dextrin (palmitic acid/ethylhexanoate), dextrin stearate and dextrin isostearate are preferable, 1 or 2 or more selected from dextrin myristate, dextrin palmitate and dextrin (palmitic acid/ethylhexanoate) are more preferable, and dextrin palmitate is still more preferable.
By combining the component (a) and the component (B) of the present invention with the other components (C) and (D), the effects of improving the removability in hot water, the flexibility of the film, and the film-forming property are achieved. It is considered that the component (B) has a hydrophilic portion and a hydrophobic portion as in the component (a), and acts as a film-forming aid in the process of fusing the components (a) to each other, resulting in improvement of film-forming properties. Further, it is considered that a soft film is formed by the interaction between the components (a) and (B), and the film is easily peeled off even when the film is removed with hot water.
Examples of commercially available dextrin fatty acid esters used as the component (B) include "Rheoseal KL2", "Rheoseal ISL", "Rheoseal TT" and "Rheoseal TL2" (manufactured by Qianya Mills Co., ltd.).
The content of the component (B) in the present invention is not particularly limited, and the lower limit value is preferably 1% or more, more preferably 2% or more, further preferably 4% or more, and particularly preferably 6% or more. The upper limit is preferably 20% or less, more preferably 15% or less, still more preferably 14% or less, and particularly preferably 12% or less. Within this range, the cosmetic properties, film flexibility, film formability, and non-halation properties when using a pen-type paint are more preferable.
In the present invention, the mass ratio of the component (a-2) to the component (B) is not particularly limited, but is preferable because a higher effect can be expected by specifying the mass ratio of the component (a-2) to the component (B). The lower limit of the content mass ratio (A-2)/(B) of the components (A-2) and (B) is preferably 0.08 or more, more preferably 0.1 or more, still more preferably 0.2 or more, and still more preferably 0.3 or more. The upper limit value is preferably 2.5 or less, more preferably 2 or less, still more preferably 1.5 or less, particularly preferably 1 or less, and most preferably 0.5 or less. Within this range, the cosmetic properties, removability in hot water, flexibility of the film, film formability, and non-halation properties when using a pen-type application are more preferable.
The component (C) in the present invention is a hydrophobized surface-treated powder, and is obtained by coating a part or all of the surface of the powder with a hydrophobized surface-treating agent in order to impart hydrophobicity to the powder. The hydrophobized surface-treated powder in the present invention is not particularly limited, and any powder can be used as long as it is generally used in cosmetics. By treating the powder, the adhesion to the surface of the powder is weakened and the aggregation of the powder is reduced, so that when the powder is combined with the component (B), a more uniform cosmetic film can be formed, and effects such as long-lasting effect can be obtained.
Examples of the surface treatment agent used in the component (C) in the present invention include fluorine compounds, silane compounds, organic titanates, silicone compounds, oils, gelling agents, emulsion polymers, and the like. In the present invention, 1 or 2 or more of them may be used in combination. Among them, from the viewpoint of excellent makeup retention and the like, 1 or 2 or more selected from a fluorine compound, a silane compound and a silicone compound are preferable, and a fluorine compound or a silane compound is more preferable, and from the viewpoint of excellent makeup retention and film flexibility, a fluorine compound is particularly preferable.
Examples of the fluorine compound in the surface treatment agent of the present invention include perfluoroalkyl phosphate diethanolamine salt, perfluorooctyltriethoxysilane, perfluoropolyether, and the like. Among them, perfluorooctyltriethoxysilane is more preferably used.
Examples of the silane compound include a silane coupling agent, and specifically, trialkoxyalkylsilane. Trialkoxyalkylsilanes are compounds in which three alkoxy groups and one alkyl group are bonded to a silicon atom, and are compounds in which the surface of a powder is chemically modified by the reaction of the alkoxy groups with hydroxyl groups and the like on the surface of the powder. The alkoxy group in the trialkoxyalkylsilane is preferably an alkoxy group having 1~3 carbon atoms, i.e., a methoxy group, an ethoxy group, a propoxy group, or the like. The alkyl group in the trialkoxyalkylsilane is preferably an alkyl group having 6 to 18 carbon atoms, such as a hexyl group, octyl group, decyl group, or octadecyl group. Examples of the trialkoxyalkylsilane include trimethoxyhexylsilane, trimethoxyoctylsilane, trimethoxydecylsilane, trimethoxyoctadecylsilane, triethoxyhexylsilane, triethoxyoctylsilane, triethoxydecylsilane, and triethoxyoctadecylsilane. Among these trialkoxyalkylsilanes, trimethoxyoctylsilane and triethoxyoctylsilane are preferable.
The amount of the hydrophobizing surface treatment agent in the hydrophobizing surface treatment powder of the component (C) of the present invention is not particularly limited, but the lower limit is preferably 0.1% or more, more preferably 0.5% or more, and still more preferably 1% or more. The upper limit is preferably 10% or less, more preferably 5% or less, and still more preferably 3% or less. Within this range, the cosmetic composition is more preferable because it is excellent not only in long-wearing properties but also in easy removal with hot water when removing the cosmetic composition and also in excellent non-staining properties when applied.
The powder used as the component (C) in the present invention is not particularly limited as long as it is a powder generally used for cosmetics, and it is not subjected to shapes such as spheres, plates, needles, etc., average particle diameters such as fine particles and pigment grades, particle structures such as porous and non-porous, etc., and examples thereof include inorganic powders, bright powders, pigment powders, metal powders, composite powders, etc. Specific examples thereof include white inorganic pigments such as titanium oxide, zinc oxide, cerium oxide and barium sulfate, colored inorganic pigments such as iron oxide, carbon black, titanium/titanium oxide sintered products, chromium oxide, chromium hydroxide, prussian blue and ultramarine blue, white inorganic pigments such as silica, talc, muscovite, phlogopite, lepidolite, biotite, synthetic mica, sericite (serite), synthetic sericite, kaolin, silicon carbide, bentonite, smectite, alumina, magnesium oxide, zirconium oxide, antimony oxide, diatomaceous earth, aluminum silicate, magnesium aluminum metasilicate, calcium silicate, barium silicate, magnesium silicate, calcium carbonate, magnesium carbonate, hydroxyapatite and boron nitride, titanium oxide-coated mica, titanium oxide-coated bismuth oxychloride, iron oxide-coated mica titanium, prussian blue-treated mica titanium, carmine-treated mica titanium, bismuth oxychloride, fish scale foil, polyethylene terephthalate/aluminum/epoxy resin laminated powder, polyethylene terephthalate/polyolefin laminated film powder, polyethylene terephthalate/polymethyl methacrylate laminated film powder, and other glittering powder, zinc stearate, aluminum stearate, magnesium stearate, zinc laurate, aluminum laurate, magnesium laurate, and other metal soaps, red 201, red 202, red 205, red 226, red 228, orange 203, orange 204, blue 404, yellow 401, red 3, red 104, red 106, orange 205, yellow 4, yellow 5, green 3, blue 1 and other zirconium, barium, or aluminum lakes, and other organic pigment powders, or further aluminum powder, gold powder, silver powder, and other metal powders, fine titanium oxide-coated mica titanium, fine zinc oxide-coated mica titanium, barium sulfate-coated mica titanium, titanium oxide-containing silica, zinc oxide-containing silica, and other composite powders.
The content of the component (C) in the present invention is not particularly limited, and the lower limit is preferably 1% or more, more preferably 5% or more, and further preferably 10% or more. The upper limit is preferably 50% or less, more preferably 30% or less, and still more preferably 20% or less. Within this range, the cosmetic properties, film flexibility, and non-staining properties when using a pen-type coating are more preferable.
In the present invention, the mass ratio of the component (B) to the component (C) is not particularly limited, but is preferable because a higher effect can be expected by specifying the mass ratio of the component (B) to the component (C). The content mass ratio (B)/(C) of the components (B) and (C) is preferably 0.1 or more, more preferably 0.2 or more, and still more preferably 0.3 or more as the lower limit. The upper limit value is preferably 2 or less, more preferably 1.5 or less, still more preferably 1 or less, and particularly preferably 0.7 or less. Within this range, the cosmetic properties, film flexibility, film formability, and non-halation properties when using a pen-type paint are more preferable.
The component (D) volatile oil agent in the present invention is an oil agent having volatility at 25 ℃. The component (D) of the present invention is not particularly limited, and the same components as the nonaqueous solvent (a-1) of the component (a) can be suitably used, and any component can be used without particular limitation as long as it is generally used in cosmetics. Specific examples thereof include volatile hydrocarbon oils and volatile silicone oils. More specifically, isododecane, light liquid isoparaffin, octamethylcyclotetrasiloxane, dodecamethylcyclohexasiloxane, methylpolytrimethylsiloxane, octylpolytrimethylsiloxane, dimethylpolysiloxane, decamethylcyclopentasiloxane, decamethyltetrasiloxane and the like are mentioned, and 1 or 2 or more of these may be contained. Among these, volatile hydrocarbon oils are preferable from the viewpoint of film-forming properties and non-blooming properties when using a pen-type coating, isododecane or light liquid isoparaffin is more preferable, and isododecane is further more preferable.
The content of the component (D) in the present invention is not particularly limited, and the lower limit is preferably 20% or more, more preferably 30% or more, and further preferably 40% or more. The upper limit is preferably 80% or less, more preferably 70% or less, and still more preferably 60% or less. Within this range, the film-forming property is more excellent, and therefore, the range is more preferable.
When the component (A-1) used in the present invention is a volatile oil, the total content [ (A-1) + (D) ] of the component (A-1) and the component (D) in the volatile oil is not particularly limited, and the lower limit is preferably 20% or more, more preferably 30% or more, and still more preferably 40% or more. The upper limit is preferably 80% or less, more preferably 75% or less, and still more preferably 70% or less. Within this range, the film-forming property is more excellent, and therefore, the range is more preferable.
In the present invention, the nonionic surfactant as the component (E) may be further contained. In the present invention, the inclusion of the component (E) is more preferable because the dispersibility of the component (C) in the eyeliner cosmetic is improved, and the eyeliner cosmetic is excellent not only in long-lasting makeup but also in removability in hot water when removing the cosmetic.
The component (E) in the present invention is not particularly limited, and the lower limit of HLB is preferably 1 or more, more preferably 2 or more, and further preferably 3 or more. The upper limit value is preferably 18 or less, more preferably 8 or less, and further preferably 5 or less. The HLB (hydrophilic-lipophilic Balance) value used in the present invention is a value obtained by the Griffin method.
The component (E) in the present invention is excellent not only in long-lasting property but also in removability in hot water upon removal of a cosmetic by specifying HLB. Further, the structure is preferably defined because the composition is excellent in non-halation properties. For example, esters of fatty acids with alcohols are preferred. The lower limit of the number of carbon atoms of the fatty acid used in the ester is preferably 12 or more, more preferably 14 or more, and still more preferably 16 or more. The upper limit of the number of carbon atoms is preferably 22 or less, more preferably 20 or less, and still more preferably 18 or less. Furthermore, it is preferred that the carbon chain of the fatty acid is branched. The alcohol is preferably a polyhydric alcohol, and more specifically, dihydric or higher alcohol, glycol, sugar alcohol, or the like can be mentioned. Among them, 1 or 2 or more selected from the group consisting of glycols, sugars and sugar alcohols are preferable, and sugars or sugar alcohols are more preferable. Examples of such sugar or sugar alcohol include glucose, sucrose, maltose, sorbitol, and the like, and 1 or 2 or more of these are preferable, sucrose or sorbitol is more preferable, and sorbitol is particularly preferable.
In the present invention, examples of the component (E) include polyoxyethylene alkyl ethers, polyoxypropylene alkyl ethers, polyoxyethylene alkylphenyl ethers, polyoxyethylene cholesterol ethers, polyoxyethylene cholestane ethers, polyoxyethylene phytosterol ethers, polyethylene glycol fatty acid esters, polyglycerol fatty acid esters, polyoxyethylene castor oil, polyoxyethylene hydrogenated castor oil fatty acid esters, sorbitan sesquioleate, polyoxyethylene sorbitan fatty acid esters, polyoxyethylene sorbitol fatty acid esters, polyoxyethylene glycerol fatty acid esters, ethylene oxide derivatives of propylene glycol fatty acid esters, ethylene oxide derivatives of polyglycerol fatty acid esters, sucrose fatty acid esters, alkylpolyglucosides, polyoxyethylene fatty acid alkanolamides, polyoxyalkylene-modified organopolysiloxanes, and polyoxyalkylene-modified organopolysiloxanes containing alkyl groups. Among them, 1 or 2 or more selected from sorbitan fatty acid esters and sucrose fatty acid esters are preferable. Specific examples thereof include sorbitan monoisostearate, sorbitan sesquiisostearate, sorbitan monopalmitate, sorbitan oleate, sorbitan sesquioleate, sorbitan tristearate, sucrose stearate, sucrose tetraisostearate, sucrose pentahydroxystearate, sucrose polystearate and the like, among which sorbitan sesquiisostearate (HLB 4), sorbitan monopalmitate (HLB 6.7), sorbitan sesquioleate (HLB 4), sucrose polystearate (HLB 1) and the like are preferable, and sorbitan sesquiisostearate, sorbitan sesquioleate, sucrose polystearate and the like are more preferable.
The content of the component (E) in the present invention is not particularly limited, and the lower limit is preferably 0.01% or more, more preferably 0.05% or more, and still more preferably 0.1% or more. The upper limit is preferably 5% or less, more preferably 3% or less, and still more preferably 1% or less. Within this range, the cosmetic properties and the non-staining properties when a pen-type application is used are more preferable because they are excellent.
In the present invention, the component (F) may further contain an organic powder. The organic powder used in the present invention is not particularly limited as long as it is an organic powder generally used in cosmetics, and is not limited to a spherical or plate-like shape, a particle size, a porous or non-porous particle structure, or the like. In the present invention, a spherical shape is preferable from the viewpoint of more excellent non-blooming property when a pen-type coating is used.
Examples of the component (F) include organic powders such as nylon powder, polymethyl methacrylate powder, acrylonitrile-methacrylic acid copolymer powder, vinylidene chloride-methacrylic acid copolymer powder, PET resin powder, polyethylene powder, polystyrene powder, organopolysiloxane elastomer powder, polymethylsilsesquioxane powder, polyurethane powder, wool powder, silk powder, crystalline cellulose, and N-acyllysine. Among them, 1 or 2 or more selected from the group consisting of organopolysiloxane elastomer powder, polymethylsilsesquioxane powder, polyurethane powder, and crystalline cellulose are preferable, 1 or 2 or more selected from the group consisting of organopolysiloxane elastomer powder, polymethylsilsesquioxane powder, and crystalline cellulose are more preferable, and 1 or 2 or more selected from the group consisting of organopolysiloxane elastomer powder and crystalline cellulose are even more preferable. Examples of commercially available organopolysiloxane elastomer powders include KSP-100, KSP-101, and KSP-102 (both manufactured by shin-Etsu chemical industries, inc., (vinyl polydimethylsiloxane/polymethylsiloxane silsesquioxane) crosspolymer).
The average particle size of the component (F) is preferably 0.1 μm or more, more preferably 1 μm or more, further preferably 3 μm or more, and particularly preferably 7 μm or more, as the lower limit value, from the viewpoint of more excellent makeup retention and non-blooming property when a pen-type coating is used. The upper limit is preferably 30 μm or less, more preferably 20 μm or less, and still more preferably 15 μm or less.
The content of the component (F) in the present invention is not particularly limited, and the lower limit is preferably 1% or more, more preferably 3% or more, and further preferably 5% or more. The upper limit is preferably 20% or less, more preferably 17% or less, and still more preferably 15% or less. When the amount is within this range, the non-staining property at the time of application is excellent, and therefore, the range is more preferable.
The eyeliner cosmetic of the present invention may further contain water. The water may be tap water, or purified water, hot spring water, deep water, etc. purified by distillation, etc. may be used. In addition, plant extractive solutions such as Aloe, witch hazel (witch hazel), hamamelis (hamamelis), fructus Cucumidis Sativi, fructus Citri Limoniae, lavender, and flos Rosae Rugosae water can also be used.
The content of water in the present invention is not particularly limited, but the lower limit is preferably 0.0001% or more, more preferably 0.001% or more, and still more preferably 0.01% or more. The upper limit is preferably 30% or less, more preferably 25% or less, and still more preferably 20% or less.
The eyeliner cosmetic of the present invention can be prepared by a generally known method.
The eyeliner cosmetic of the present invention is not particularly limited, and may take the form of powder, solid, liquid, gel, etc., and is preferably liquid or gel from the viewpoint of non-halation property when a pen-type application is used or when a pen-type application is used. The eyeliner cosmetic of the present invention may be of an oil type or an aqueous type, and among them, an oil type is preferable. The oily type includes nonaqueous type and W/O type. In the present specification, the nonaqueous type means a type in which the content of water is 5% or less, preferably 3% or less, and more preferably 1% or less. The oily eyeliner cosmetic of the present invention is an oily type, but has the advantage of being excellent in removability in hot water of an aqueous type.
The eyeliner cosmetic of the present invention is not particularly limited, and can be prepared in various viscosities. For example, the lower limit value is preferably 250 mPas or more, more preferably 500 mPas or more, and still more preferably 1000 mPas or more at 25 ℃. The upper limit is preferably 20000 mPas or less, more preferably 18000 mPas or less, and still more preferably 15000 mPas or less at 25 ℃. In the present invention, the viscosity at 25 ℃ can be measured according to the second method of measurement of viscosity of cosmetic raw materials using a Brookfield viscometer. For example, the eyeliner cosmetic can be left to stand at 25 ℃ for 1 day, and measured with a brookfield viscometer (product of british herbal and herbal medicine) under the following conditions: the measurement was performed at 25 ℃ for 1min at a measurement time of 6rpm using a rotor No. 4.
Examples
The present invention will be described in more detail below with reference to examples. It should be noted that they do not limit the present invention in any way.
Examples 1 (inventive products 1 to 27) and comparative examples (comparative product 1~6): eye line
Eye liner shown in preparation table 1~4 was evaluated for a. Long wear, b. Removability in hot water, c. Film flexibility, d. Film formability, and e. Non-tingling property upon application by the following evaluation methods. The results are also shown in Table 1~4.
[ Table 1]
Figure DEST_PATH_IMAGE002
In addition, the method is as follows: nissetsu U-3712A (Nippon Carbide Industry Co., ltd., solid content 45% isododecane solvent)
Alkyl (meth) acrylates (Tg 30 ℃ C.: vinyl acetate 50
In addition, 2: the composition of the copolymer is the same as that of the corresponding color 1 (solid content 45% of isododecane solvent)
Alkyl (meth) acrylate (Tg 30 ℃: vinyl acetate = 70)
The color is about 3: the composition of the copolymer is the same as that of the corresponding color 1 (solid content 45% of isododecane solvent)
Alkyl (meth) acrylate (Tg 30 ℃: vinyl acetate = 30)
In addition, 4: rheopearl KL2 (manufactured by Qianye Mills Co.): degree of substitution 2
In addition, the method is as follows: rheopearl TL2 (manufactured by Qianye Mill Co.): degree of substitution 1.5
In addition, 6: rheopearl MKL2 (manufactured by Qianye Mills Co.): degree of substitution: 2
In addition, the color is 7: rheopearl TT2 (manufactured by Qianye Mill Co., ltd.): degree of substitution 1.5
And (2) separately: KF-96L-2CS (manufactured by shin-Etsu chemical industries Co., ltd.)
The color is about 9: KSP-100 (manufactured by Xinyue chemical industry Co., ltd.)
In addition, the color is 10: KSP-101 (manufactured by shin Yue chemical industry Co., ltd.)
The method is characterized in that: KSP-102 (manufactured by Xinyue chemical industry Co., ltd.)
The method is characterized by being in color in 12: CELLULOBEADS D-10 (Dazai Kagaku Co., ltd.).
[ Table 2]
Figure DEST_PATH_IMAGE004
[ Table 3]
Figure DEST_PATH_IMAGE006
[ Table 4]
Figure DEST_PATH_IMAGE008
(preparation method)
A. The components (1) to (22) and (27) were heated to 80 ℃ and mixed uniformly.
B. Process a with a roller.
C. Ingredients (23) to (26) were added to B, mixed, and then filled in a container with a pen-type coating to obtain an eyeliner.
(evaluation items)
a. Make-up keeping property
c. Flexibility of film
e. No halation when applied.
(evaluation method)
Using example 1 (present invention products 1 to 27) and comparative example (comparative example 1~6) from 20 cosmetic evaluation professional panelists, with respect to (a), whether or not the cosmetic film remained without changing after 8 hours, and with respect to (c), there was no feeling of burden upon blinking (following the movement of blinking, the cosmetic film also moved flexibly without feeling a feeling of burden, and it was judged that there was flexibility of the film), and with respect to (e), whether or not the cosmetic film was drawn with a pen-type paint without staining, and the panelists were each evaluated and scored on a 4-point scale according to the following evaluation criteria, and the average score of the scores of all panelists was judged according to the following evaluation criteria.
(evaluation criteria)
(score): (evaluation)
4: is very good
3: good effect
2: difference between
1: very poor.
(criteria for determination)
(judgment): (average score of scores)
Very good: 3.5 min or more
Good: 3.0 min or more and less than 3.5 min
And (delta): 2.0 min or more and less than 3.0 min
X: less than 2.0 minutes.
(evaluation items)
b. Easy removability in hot water.
(evaluation method)
After the evaluation of makeup retention was completed, 20 cosmetic evaluation professional panelists used example 1 (products 1 to 27 of the present invention) and comparative example (comparative product 1~6) and wiped them with hot water at 40 ℃ 5 or more times to evaluate removability in hot water, and the evaluation was made according to the following criteria.
(determination criteria)
(judgment): (case of washing with Hot Water)
Very good: scrubbing with 40 deg.C hot water for 5 times, and completely removing
O: scrubbing with hot water of 40 ℃ for 6 to 10 times, and completely removing
And (delta): scrubbing with hot water of 40 ℃ for 11 to 15 times, and completely removing
X: when the skin is scrubbed with hot water of 40 ℃ for more than 16 times, the cosmetic film remains.
(evaluation items)
d: film forming property
(evaluation method)
0.2g of each of example 1 (invention products 1 to 27) and comparative example (comparative example 1~6) was drawn out on a glass plate to an area of 3cm × 3cm and a thickness of 12.5 μm, and the time taken until no lump (bulk) was attached to the finger when the surface of the film was touched with the finger was determined according to the following criteria for confirming that the coating film was dried and formed.
(criteria for determination)
(judgment): (time required until the coating film is dried)
Very good: the coating film is dried within 1 minute and 30 seconds after being coated
Good: the coating film is dried at 1min 30 sec or more and less than 2 min 30 sec after application
And (delta): the coating film is dried 2 minutes 30 seconds or more and less than 3 minutes 30 seconds after being applied
X: the coating film is dried for more than 3 minutes and 30 seconds after being coated
From the results of table 1~4, the eyeliner of example 1 (products 1 to 27 of the present invention) is superior to the comparative example in all of the items of makeup durability, easy removability in hot water, flexibility of film, film formability, and non-halation property at the time of application. On the other hand, comparative products 1 and 2, in which component (A) was replaced with another polymer or resin, were deficient in removability in hot water, flexibility of film, and film-forming property. Comparative products 3, 4 and 5, in which component (B) was replaced with another thickener and the viscosity was adjusted to the same level as that of inventive product 3 (25 ℃ C., 15000 mPas), were also deficient in long-wearing properties, film flexibility, film-forming properties, and freedom from staining when using a pen-type coating. Comparative product 6, which used the powder without surface treatment, was deficient in long-wearing properties, film flexibility and film-forming properties.
Example 2 eyeliner liquid
Figure DEST_PATH_IMAGE010
(preparation method)
A. Heating the components (1) - (15) to 80 ℃, and uniformly mixing.
B. Process a with a roller.
C. The ingredients (16) and (17) were added to B, mixed, and then filled in a container with a pen-type application to obtain an eyeliner.
The liquid eyeliner thus obtained is excellent in the makeup-holding property, the removability in hot water, the flexibility of the film, the film-forming property, and the non-staining property when a pen-type application is used.
EXAMPLE 3 eyeliner gel
Figure DEST_PATH_IMAGE012
(preparation method)
A. Heating the components (1) to (13) to 80 ℃, and uniformly mixing.
B. Process a with a roller.
C. The ingredient (14) was added to B, mixed, and then filled in a container with a pen-type application to obtain an eyeliner.
The gel-like eyeliner obtained as described above is excellent in the makeup-holding property, the removability in hot water, the flexibility of the film, the film-forming property, and the non-tingling property when using a pen-type application.
EXAMPLE 4 eyeliner solid State
Figure DEST_PATH_IMAGE014
A. The components (1) to (15) were dissolved uniformly at 100 ℃.
B. Add ingredient (16) to a and mix well.
C. And B is dissolved and filled in a metal dish at 90 ℃, and is cooled and solidified to obtain the solid eyeliner.
The eyeliner filled in the metal dish obtained as described above is excellent in the makeup-holding property, the removability in hot water, the flexibility of the film, the film-forming property, and the non-tingling property when the pen-type spread is used.
Example 5 eyeliner Water-in-oil type emulsion cosmetic
Figure DEST_PATH_IMAGE016
A. The components (1) to (8) were dissolved uniformly at 80 ℃.
B. The components (9) to (18) were added to A, and the mixture was uniformly emulsified.
C. Adding the component (19) into the mixture B, uniformly mixing, and filling into a container with pen-shaped coating to obtain the eyeliner.
The eyeliner obtained as described above is excellent in the makeup durability, removability in hot water, flexibility of film, film formability, and freedom from staining when using a pen-type application.

Claims (12)

1. An eyeliner cosmetic comprising the following components (A) to (D):
(A) (A-2) an alkyl acrylate/vinyl acetate copolymer dispersion using (A-1) a nonaqueous solvent as a dispersion medium,
(B) Dextrin fatty acid ester,
(C) A hydrophobized surface-treated powder,
(D) A volatile oil agent.
2. The eyeliner according to claim 1, wherein the component (A-2) acrylic alkyl ester/vinyl acetate copolymer is obtained by copolymerizing an alkyl (meth) acrylate and vinyl acetate in a mass ratio of 30 to 95.
3. The eyeliner cosmetic according to claim 1 or 2, wherein the Tg of the polymer of the alkyl (meth) acrylate constituting the component (A-2) alkyl acrylate/vinyl acetate copolymer is 10 ℃ or higher and 50 ℃ or lower.
4. The eyeliner cosmetic of any one of claims 1~3 wherein component (A-2) alkyl acrylate/vinyl acetate copolymer has a number average molecular weight of 5 to 50 ten thousand.
5. The eyeliner cosmetic according to claim 1~4, wherein the content of said component (A-2) is 0.8 to 20% by mass.
6. The eyeliner cosmetic of any one of claims 1~5 wherein said ingredient (B) is dextrin palmitate.
7. The eyeliner cosmetic of any one of claims 1~6, wherein said component (C) is a fluorine compound surface-treated powder.
8. The eyeliner cosmetic according to claim 1~7, wherein the contents mass ratio (A-2)/(B) of said components (A-2) and (B) is 0.08 to 2.5.
9. The eyeliner cosmetic of any one of claim 1~8 further comprising ingredient (E) a nonionic surfactant.
10. The eyeliner cosmetic of claim 1~9, further comprising component (F) organic powder.
11. The eyeliner according to claim 9, wherein the component (E) is an ester of a branched fatty acid having 16 to 20 carbon atoms and a sugar alcohol.
12. The eyeliner cosmetic according to claim 10, wherein the component (F) is an organic spherical powder.
CN202180025766.3A 2020-03-30 2021-03-23 Eyeliner cosmetic Pending CN115297834A (en)

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