GB2196978A - Nail-strengthening cosmetic compositions - Google Patents

Nail-strengthening cosmetic compositions Download PDF

Info

Publication number
GB2196978A
GB2196978A GB08722647A GB8722647A GB2196978A GB 2196978 A GB2196978 A GB 2196978A GB 08722647 A GB08722647 A GB 08722647A GB 8722647 A GB8722647 A GB 8722647A GB 2196978 A GB2196978 A GB 2196978A
Authority
GB
United Kingdom
Prior art keywords
nail
glyoxal
nails
strengthening
nitrocellulose
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
GB08722647A
Other versions
GB8722647D0 (en
GB2196978B (en
Inventor
Harold Suss
James Edward Doyle
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer Consumer Care Holdings LLC
Original Assignee
Plough Inc
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
Application filed by Plough Inc filed Critical Plough Inc
Publication of GB8722647D0 publication Critical patent/GB8722647D0/en
Publication of GB2196978A publication Critical patent/GB2196978A/en
Application granted granted Critical
Publication of GB2196978B publication Critical patent/GB2196978B/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q3/00Manicure or pedicure preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q3/00Manicure or pedicure preparations
    • A61Q3/02Nail coatings

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)

Abstract

A cosmetic composition comprises an amount of glyoxal sufficient to strength nails in admixture with a substantially non-aqueous conventional nitrocellulose-based nail lacquer preperation. The nail lacquers can be clear and colorless or can have pigments therein. The preferred amount of glyoxal is about 0.001 to about 1.00 weight percent of the composition.

Description

SPECIFICATION Nail strengthening compositions and method of using same This invention relates to cosmetic nail strengthening compositions. The compositions may be clear or colored with conventional organic and inorganic pigments. The invention also contemplates a method of strengthening nails by applying the inventive compositions to the nails.
Many users or would-be users of nail polish have difficulty due to cracked, split or broken toe nails and finger nails. The cause of these conditions has been attributed to one of more of the following: the use of nail polish and/or nail polish remover, the use of soap or detergents, and/or a natural idosyncrasy of the user.
Numerous nail preparations have been made which claim to strengthen nails by the action of chemicals contained in them. Nail hardening compositions in which the principal active component is formaldehyde in a concentration generally ranging from 4 to 15% have been proposed.
See for example, U.S. Patent 3,382,151 (Knudein). However, the use of formaldehyde in cosmetics produces undesirable side effects, such as inflammation, hardening and/or formation of horn on adjacent skin areas. In addition, the formaldehyde has a rather dangerous toxic effect, especially on the nerve cells of the skin and the capillaries. Accordingly, the U.S. Food and Drug Administration considers any solution which contains more than 4% formaldehyde to be "a poisonous or deleterious substance." Numerous nail strengtheners have been proposed to overcome the problems associated with using formaldehyde.
UK Patent 1,183,513 (issued March 11, 1970) discloses compositions for treating nails containing one or more mono-aldehydes containing at least two carbon atoms or polyaldehydes containing more than two carbon atoms. U.S. Patents 3,349,000 and 3,725,525 disclose that use of the reaction product of formaldehyde with thiourea imparts to native keratins, e.g., nails, higher elasticity and strength than do free aldehydes without producing any undesirable side effects. U.S. Patent 382,151 discloses the use of a nail strengthening composition containing a high concentration of formaldehyde modified by vegetable extracts.
French Patent 1,485,602 (Morelle) discloses nail polish compositions containing aqueous solutions of glyoxal in combination with acylated protein derivatives.
U.S. Patents Nos. 4,296,104, 4,296,130 and 4,447,469 disclose nail conditioner and nail polish compositions containing glyoxal, high concentrations of water in admixture with methylsulfonylmethane (MSM), dimethylsulfoxide (DMSO) and carbimide or urea. However, MSM is disclosed as the active ingredient and DMSO is described as accelerating the penetration of MSM and urea or carbimide into the tough nail material.
U.S. Patents Nos. 4,256,768 and 4,569,946 disclose topical application of diiute aqueous or alcoholic solutions of lower dialdehydes such as glyoxal to human tissue for treatment of gangrene, burns and raw, cut portions of the body during surgical excision of malignant tumors.
Nothing regarding nail strengthening compositions is recited.
There is a need for a nail strengthening composition that operates to strengthen nails efficiently and safely without causing the undesirable side effects experienced with prior art compositions.
The present invention is summarized as a cosmetic composition for strengthening nails comprising an amount of glyoxal effective for strengthening nails in a substantially non-aqueous conventional nitrocellulose-based nail lacquer preparation. The invention also provides a method of strengthening the nails which comprises applying to the nails a cosmetic composition comprising an amount of glyoxal sufficient to strengthen said nails in admixture with a substantially non-aqueous conventional nitroceilulose-based nail lacquer preparation, which preparation- may be colorless or colored with conventional nail polish organic and inorganic pigments.
Glyoxal is a dialdehyde having the formula
and is commercially available as a 40% aqueous solution which also contains a polymerization inhibitor. Vacuum evaporation of the aqueous glyoxal solution leads to polyglyoxal, a trimer of glyoxal. Thermal depolymerization of polyglyoxal in the presence of drying agents yields unstable anhydrous monomeric glyoxal which must be used immediately. See for example G. Mattioda, et al., CHEMTECH, August 1983 pp. 478-481. Thus, while aqueous or anhydrous glyoxal may be used in the compositions and process of the present invention, the use of 40% aqueous glyoxal solutions is more convenient.
As used throughout the present specification and claims, all percentages are weight percents unless stated otherwise.
Percentages of "glyoxal" in the compositions are based a 40% aqueous glyoxal solution, hence to obtain the percentage of dry glyoxal, multiply each percentage of "glyoxal" by 0.40.
Of course the claims are intended to cover compositions prepared using solutions of glyoxal having different concentrations when said compositions contain the same amount of glyoxal on a dry basis.
The amount of glyoxal in the cosmetic composition of the present invention found effective for strengthening nails when added to a substantially non-aqueous conventional nitrocellulose-based nail lacquer preparation is about 0.001 to about 1.0 weight percent, preferably about 0.001 to about 0.25 weight percent, more preferably about 0.01 to about 0.25 weight percent of the cosmetic composition. By employing these amounts of glyoxal in said nail lacquer preparation in accordance with the present invention, nail strengthening is effected without the deleterious side effects associated with prior art formaldehyde-containing preparations.
The term "substantially non-aqueous" as used herein means less than about 1 weight percent water. With the exception of the small amount of water introduced by addition of glyoxal as a 40% aqueous glyoxal solution, no water should be intentionally added in the preparation of the cosmetic compositions of the present invention. However, the solvents and other components of the conventional nitrocellulose-based nail lacquer preparations need not be completely anhydrous for use in the cosmetic compositions and process of the present invention, provided the final composition is substantially non-aqueous as defined in this paragraph.
Conventional nitrocellulose-based nail lacquer preparations have been found useful in the present invention. Typical suitable conventional nitrocellulose-based nail lacquer preparations include: Nitrocellulose (7-25%, more preferably 10-18%, and most preferably 12-16%), secondary resins (5-15%), plasticizers (2-8%), and solvents (55-80%, more preferably 60-80%).
Other optional ingredients include: Thickening and suspending agents, UV light masking and sunscreening agents, Colorants, and Decorative materials.
Nitrocellulose is the primary film-former used in the typical nail lacquer preparation and should have a viscosity value (R/S Value) of from 1/4 to 5/6 seconds (enabling the manufacture of cosmetic nail strengthening compositions that flow readily and are capable of producing a film with sufficient gloss in one application), and be perfectly neutral, for free acid may damage the finger nail and destroy the pigments used in tinting the nail lacquer preparation.
Typical suitable secondary resins compatible with nitrocellulose include most natural resins such as Benzoin, Dammar, Ester gum, Pontianac Sandara or Shellac and any synthetic resin such as the alkyd, acrylate- and methacrylate-based resins, polyester resins (Lipo Rez resins) and formaldehyde sulfonamide resins (Santolite resins). Santolite resin in combination with acrylate copolymer resins, is a preferred secondary resin. Other secondary resins include: nylon. available under the tradename of Versamid 930 from Henkel, Inc., Teaneck, NJ 07666, acrylates copolymer resins, available from Rhom and Haas Co., Philadelphia, PA 19105, under the tradename of Acryloid B-66, and styrene/acrylate/acrylonitrile copolymers, available from Dow Chemical U.S.A., Midland, Ml 48640.
Typical suitable plasticizers include blown castor oil, camphor, raw castor oil, dibutyi phthalate and tricresyl phosphate. Use of a combination camphor and at least one or two other plasticizers, normally dibutylphthalate and/or sucrose acetate isobutyrate is conventional.
UV light masking agents used in clear nail laquer compositions to mask the yellow color caused by discoloration of the nitrocelluose resin include pigments such as D & Violet #2.
Typical suitable sunscreening agents include esters of para-aminobenzoic acid and substituted para-aminobenzoic acid, e.g., octyl dimethyl PABA; certain esters of salicylic acid, e.g., homomethyl salicylate; certain benzophenone derivatives, such as benzophenone-1 or -3; and the esters of para-methoxycinnamic acid, e.g., octyl methoxycinnamate.
The compositions of the present invention may also include thickening and suspending agents for the colorants. Typical suitable thickening and suspending agents include stearalkonium Hectorite, a reaction product of Hectorite (one of the montmorillonite minerals that are the principal constituents of bentonite clay) and stearalkonium chloride [a quarternary ammonium salt of the formula, + [CH3(CH) 5CH2-N-(CH3)2-CH2-C6H5jCl].
Typical suitable decorative materials include aluminum polyester terephthalate, available under the tradename Bril Chrome Silver from Meadowbrook Inventions, Bernardsville, NJ 07924; acrylates copolymer and polybutene terephthalate and ethylene/vinyl acetate copolymer available under the tradename Crystalina from Meadowbrook Inventions; Silver available under the trade- name Silver from Presperse, Inc. So. Piainfield, N.J. 07080; decorative pearl available under the tradename Mearlmaid from Mearl Corp. NY, NY 10017; mica; titanium dioxide coated mica; bismith oxychloride and guanine.
The solvent combination found suitable in conventional nitrocellulose-based nail lacquer preparations consists of an alcohol, such as ethanol or iso-propyl alcohol which is used to wet the nitrocellulose, together with an active solvent such as n-, sec- or iso-butyl acetate or ethyl acetate and an aromatic hydrocarbon diluent such as toluene or xylene. Other typical suitable solvents are found on pages 991-994 of "Nail Preparations" by Henry J. Wing, Chapter 49, pp.
983 to 1110, in "The Chemistry and Manufacture of Cosmetics", Second Edition, Volume IV edited by M. G. deNavarre, Continental Press, 1975, Orlando, Florida which is hereby incorporated by reference.
The conventional nitrocellulose-based nail lacquer preparation may be clear or colorless, i.e.
unshaded or shaded. The shaded product may contain insoluble organic and inorganic colorants together with small proportions of titanium dioxide. The organic colorants should be selected from an FDA approved list of certified pigments and dyes; the inorganic pigments should conform to the FDA specifications with respect to heavy metal content. A listing of the opaque and transparent colorants is given on pp. 997-998 of "Nail Preparations" cited hereinabove.
The process of the present invention consists of strengthening finger or toe nails, by applying to the surface thereof using a conventional nail polish applicator, a cosmetic composition such as described above or in the examples.
The following examples further describe and illustrate formulation of representative unshaded and shaded nitrocellulose-based nail lacquer preparations. All of the mixing operations of the examples were performed at room temperature.
The nitrocellulose was obtained from Hercules, Inc., Wilmington, DE 19899; the toluene sulfonamide/formaldehyde resin tradenamed Santolite resins from Monsanto Chemical Co., St.
Louis, MO 63116; benzophenone-1 is a UV sunscreening agent from BASF Wyandotte Corp., Parsippany, NJ 07054; isostearic hydrolyzed animal protein is a conditioning agent available under the tradename Crotein IPX from CRODA, NY, NY 10010; polyester resins available under the tradename Lipo Rez resins from Lipo Chemicals, Inc. Paterson, NJ 07504; and stearalkonium Hectorite is a thickening and suspending agent available from NL Chemicals Division of NL Industries, Highstown, NJ 08520.
The suppliers of other ingredients used in the following illustrative examples are well known and can be found, e.g. in CTFA Cosmetic Ingredient Dictionary, Third Edition, 1982, N.F. Estrin et al., eds., published by The Cosmetic, Toiletry and Fragrance Association, Inc., 1110 Vermont Avenue, N.W., Washington, D.C. 20005.
EXAMPLE 1 Colorless Nail Lacquer Composition Ingredient Weight % Butyl Acetate 26.00 Toluene 20.00 Nitrocellulose R/S 1/2 sec. 14.00 Isopropyl Alcohol 5.00 Toluene Sulfonamide Formaldehyde Resin 10.00 Ethyl Acetate 19.599 Camphor 0.50 Benzophenone-1 0.10 Nylon 0.10 Acrylates Copolymer 0.10 Sucrose Acetate Isobutyrate 4.00 Polyester Resin 0.50 Glyoxal 0.001 D & Violet No. 2, (0.01% solution 0.10 Total 100.000 To a stainless steel kettle equipped with a high shear stirrer, charge the toluene, toluene sulfonamide/formaldehyde resin, butyl acetate and one half of the ethyl acetate and stir until a homogeneous mixture is formed. Continue to stir and slowly add to the mixture the nitrocellu lose, benzophenone-1, camphor and sucrose acetate isobutyrate.To the stirred homogeneous mixture so formed, add nylon, acrylates copolymers, polyester resin and continue stirring until a homogeneous mixture is reformed. Continue stiring and add the isopropyl alcohol, D & violet #2, remaining half of ethyl acetate, and glyoxal. Fill into bottles.
EXAMPLE 2 Colorless Nail Lacquer Composition Ingredient Weight % Butyl Acetate 18.26 Toluene 25.40 Nitrocellulose R/S 1/2 sec. 14.00 Isopropyl Alcohol 1.00 Toluene Sulfonamide Formaldehyde Resin 10.00 Dibutyl Phthalate 4.00 Ethyl Acetate 25.60 Camphor 0.99 Benzophenone- 1 0.10 Nylon 0.10 Acrylates Copolymer 0.10 Glyoxal 0.25 D & Violet No. 2, (0.01% solution) 0.10 Isostearic Hydrolyzed Animal Protein 0.10 Total 100.000 Following the procedure of Example 2 except add the dibutylphthalate to the mixture containing nitrocellulose and add the isostearic hydrolyzed animal protein to the mixture containing nylon.
EXAMPLES 3 AND 4 Colored Nail Polish Ingredients Weight % Part A Example 3 Example 4 Toluene 25.10 25.45 Toluene Sulfonamide/Formaldehyde Resin 9.00 0.05 Butyl Acetate 25.33 25.66 Part B Nitrocellulose R/S 1/2 sec. 14.00 14.00 Stearalkonium Hectorite 1.30 1.30 Benzophenone- 1 0.10 0.10 Dibutyl Phthalate 2.50 0.05 Camphor 2.00 2.00 Polyester Resin 2.50 10.00 Sucrose Acetate Isobutyrate 2.50 2.50 Part C Nylon 0.10 0.10 Acrylates Copolymer 0.10 0.10 Styrene/Acrylate/Acrylonitrile Copolymer 0.05 0.05 Part D Ethyl Acetate 4.00 5.00 Isopropyl Alcohol 10.00 10.00 Butyl Alcohol 1.00 3.00 SD-Alcohol-3A 0.05 0.05 Glyoxal 0.01 0.01 Part E Titanium Dioxide 0.20 0.04 D & Red No. 7 Calcium Lake 0.05 0.09 Iron Oxides 0.08 0.05 D & Red No. 6 Barium Lake 0.02 0.20 Ferric Ammonium Ferrocyanide 0.01 Bismith Oxychloride, 11 % 0.20 Total 100.00 100.0 To an appropriate stainless steel kettle equipped with a high shear stirrer, charge the ingredients in Part A and stir until a homogeneous mixture is formed. Slowly add to the so formed mixture the ingredients in Part B. Stop stirring and cover kettle to prevent evaporation of solvents and hold so formed homogeneous mixture for 10 hours. Remove cover, stir and add the ingredients of Part C. To the so formed homogeneous mixture, add the ingredients in Part D.
To the homogeneous mixture so formed add the ingredients in Part E and stir until a homogeneous mixture is formed.

Claims (6)

1. A cosmetic composition for strengthening nails comprising an amount of glyoxal effective for strengthening nails in a substantially non-aqueous conventional nitrocellulose-based nail lacquer preparation.
2. The composition of claim 1 containing from 0.001 to 1 percent glyoxal.
3. The composition of claim 2 containing from 0.001 to 0.25 percent glyoxal.
4. The composition of any one of claims 1 to 3 wherein the sub-stantially non-aqueous conventional nitrocellulose-based nail lacquer comprises.
(a) 7 to 25% nitrocellulose, (b) 5 to 15% secondary resins, (c) 2 to 8 plasticizers, and (d) 55 to 80% solvents.
5. A method of strengthening nails comprising applying to the nails the composition of anyone of claims 1 to 3.
6. A method of strengthening nails comprising applying to the nails the composition of claim 4.
GB8722647A 1986-09-25 1987-09-25 Cosmetic nail strengthening compositions and method of using same Expired - Fee Related GB2196978B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US91156386A 1986-09-25 1986-09-25

Publications (3)

Publication Number Publication Date
GB8722647D0 GB8722647D0 (en) 1987-11-04
GB2196978A true GB2196978A (en) 1988-05-11
GB2196978B GB2196978B (en) 1990-04-18

Family

ID=25430472

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8722647A Expired - Fee Related GB2196978B (en) 1986-09-25 1987-09-25 Cosmetic nail strengthening compositions and method of using same

Country Status (3)

Country Link
JP (1) JPS6391314A (en)
AU (1) AU603138B2 (en)
GB (1) GB2196978B (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2251437A (en) * 1990-12-28 1992-07-08 Juniper Weikop Product Dev Ltd A sprayable composition for application to a fabric
WO1999036033A1 (en) * 1998-01-14 1999-07-22 Woodward Laboratories, Inc. Antimicrobial nail coating composition
FR2805745A1 (en) * 2000-03-01 2001-09-07 Bergerac Nc Antifungal and antibacterial nail varnish for the treatment of fungal nail infections, consists of a nitrocellulose in organic solvent and formalin
FR2819402A1 (en) * 2001-01-17 2002-07-19 Oreal Composition useful for making nail varnish sticks comprises liquid phase including volatile organic solvent thickened with specified polymer
US6716420B2 (en) 2001-10-05 2004-04-06 L′Oreal Methods of use and of making a mascara comprising at least one coloring agent and at least one heteropolymer
US6835399B2 (en) 2000-12-12 2004-12-28 L'ORéAL S.A. Cosmetic composition comprising a polymer blend
US7749524B2 (en) 2003-07-11 2010-07-06 L'oreal S.A. Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent
US8080257B2 (en) 2000-12-12 2011-12-20 L'oreal S.A. Cosmetic compositions containing at least one hetero polymer and at least one film-forming silicone resin and methods of using
US9211242B2 (en) 2009-03-30 2015-12-15 Fiabila Nail-hardening cosmetic composition, use of aldehydes to harden and strengthen nails, and method for applying same
WO2019207249A1 (en) 2018-04-25 2019-10-31 Fiabila Cosmetic composition of non-aqueous thixotropic nail varnish containing a nail-hardening agent, use and implementation method
WO2021234270A1 (en) 2020-05-19 2021-11-25 Fiabila Cosmetic nail care composition in the form of a varnish

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2586764B2 (en) * 1991-08-09 1997-03-05 日本ターナー株式会社 Manicure products using aromatic paints
US8333956B2 (en) 2002-06-11 2012-12-18 Color Access, Inc. Stable cosmetic emulsion with polyamide gelling agent
US8449870B2 (en) 2002-06-11 2013-05-28 Color Access, Inc. Stable cosmetic emulsion with polyamide gelling agent
JP5431660B2 (en) * 2007-08-31 2014-03-05 株式会社コーセー Beauty nail

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ211547A (en) * 1984-06-29 1988-05-30 Chesebrough Ponds Nail polish and applicator

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2251437A (en) * 1990-12-28 1992-07-08 Juniper Weikop Product Dev Ltd A sprayable composition for application to a fabric
WO1999036033A1 (en) * 1998-01-14 1999-07-22 Woodward Laboratories, Inc. Antimicrobial nail coating composition
FR2805745A1 (en) * 2000-03-01 2001-09-07 Bergerac Nc Antifungal and antibacterial nail varnish for the treatment of fungal nail infections, consists of a nitrocellulose in organic solvent and formalin
US6835399B2 (en) 2000-12-12 2004-12-28 L'ORéAL S.A. Cosmetic composition comprising a polymer blend
US8080257B2 (en) 2000-12-12 2011-12-20 L'oreal S.A. Cosmetic compositions containing at least one hetero polymer and at least one film-forming silicone resin and methods of using
FR2819402A1 (en) * 2001-01-17 2002-07-19 Oreal Composition useful for making nail varnish sticks comprises liquid phase including volatile organic solvent thickened with specified polymer
WO2002056848A1 (en) * 2001-01-17 2002-07-25 L'oreal Nail varnish comprising a polymer
US6716420B2 (en) 2001-10-05 2004-04-06 L′Oreal Methods of use and of making a mascara comprising at least one coloring agent and at least one heteropolymer
US7749524B2 (en) 2003-07-11 2010-07-06 L'oreal S.A. Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent
US9211242B2 (en) 2009-03-30 2015-12-15 Fiabila Nail-hardening cosmetic composition, use of aldehydes to harden and strengthen nails, and method for applying same
WO2019207249A1 (en) 2018-04-25 2019-10-31 Fiabila Cosmetic composition of non-aqueous thixotropic nail varnish containing a nail-hardening agent, use and implementation method
WO2021234270A1 (en) 2020-05-19 2021-11-25 Fiabila Cosmetic nail care composition in the form of a varnish
FR3110412A1 (en) 2020-05-19 2021-11-26 Fiabila Cosmetic nail care composition in the form of a varnish

Also Published As

Publication number Publication date
GB8722647D0 (en) 1987-11-04
GB2196978B (en) 1990-04-18
AU603138B2 (en) 1990-11-08
JPS6391314A (en) 1988-04-22
AU7899887A (en) 1988-03-31

Similar Documents

Publication Publication Date Title
AU603138B2 (en) Nail strengthening composition and method for using same
US5264206A (en) Nail lacquer with antimycotic activity, and a process for the preparation thereof
US4980155A (en) Two phase cosmetic composition
US4957730A (en) Antimycotic nail varnish
CA1294554C (en) Cosmetic composition for skin coloration containing mesotartaric aldehyde and one or more hydroxyquinones, and process for the coloration of skin withthis composition
US4264581A (en) Sunscreen composition
JP2859583B2 (en) Nail treatment composition containing hydroxycarboxylic acids
EP0223257B1 (en) Hair stabilizing composition
CA1101336A (en) Ester of alkylvinylether/maleic anhydride copolymer in plasticized nail enamel
US4032464A (en) Creamy nail lacquer remover
JP2002513741A (en) Nail polish kit
JP2983537B2 (en) Nitrocellulose-based cosmetic vanish composition containing stabilizer
EP0072298B1 (en) Extemporaneous cosmetic preparation with dyeing capability, in particular for capillary use
JPH0660089B2 (en) Hair dye cosmetics
US20080112908A1 (en) Anti-fungal nail lacquer
JPH01149708A (en) Hair-treatment composition
JP2001506647A (en) Use of Okume resin extract in cosmetics and pharmaceuticals, especially in dermatology
CA1222461A (en) Hair spray composition
KR20180108266A (en) Composition for dyeing
US5466441A (en) Nail polish drying method
DE19818837A1 (en) Acylated peptide and cosmetic product containing it
CA1298790C (en) Fingernail cosmetic composition
JPS62226910A (en) Skin cosmetic
Schlossman Manicure preparations
EP1447076A1 (en) Use of fullerene solutions for conditioning hair

Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee

Effective date: 20060925