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WO2018102195A1 - Nail coating remover - Google Patents

Nail coating remover Download PDF

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Publication number
WO2018102195A1
WO2018102195A1 PCT/US2017/062748 US2017062748W WO2018102195A1 WO 2018102195 A1 WO2018102195 A1 WO 2018102195A1 US 2017062748 W US2017062748 W US 2017062748W WO 2018102195 A1 WO2018102195 A1 WO 2018102195A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
nail
organic solvent
boiling point
volatile organic
Prior art date
Application number
PCT/US2017/062748
Other languages
French (fr)
Inventor
Robert SANDEWICZ
Original Assignee
Revlon Consumer Products Corporation
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 Revlon Consumer Products Corporation filed Critical Revlon Consumer Products Corporation
Publication of WO2018102195A1 publication Critical patent/WO2018102195A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q3/00Manicure or pedicure preparations
    • A61Q3/04Nail coating removers
    • 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
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/362Polycarboxylic acids
    • 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
    • A61K8/37Esters of carboxylic acids
    • 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
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30Characterized by the absence of a particular group of ingredients
    • A61K2800/31Anhydrous

Definitions

  • the present disclosure relates generally to a composition for nail coating remover, and particularly, but .not by way of limitation, a combination of ingredients that improve removal of difficult enamels and glitters used in nail coating on the naii.
  • Contemporary nail coatings use higher performance polymers, higher levels of pigments, alternative pigments (e.g. blues and blacks); glitters, and photo-reactive nail coatings to provide a durable scratch resistant nail coating with improved adhesion. These contemporary nail coatings are longer lasting and difficult to remove with the traditional nail coating removers currently on the market.
  • a composition that is substantially anhydrous composition comprises at least one of a volatile organic solvent with an atmospheric boiling point of about 55 ⁇ 80oC, at least one of a volatile organic solvent with atmospheric boiling point > 240'C, and at least one of a di-basic ester.
  • the volatile organic solvent with an atmospheric boiling point of about 55 - 80oC Is an acetone or acetate.
  • a non-iimiting example of the volatile organic solvent with atmospheric boiling point > 240oC is propylene carbonate.
  • a non-limiting example of the dibasic ester is diethylhexyl maieate.
  • composition when applied, to a dried nati teaching on natural or synthetic nails removes the nail coating with ⁇ 12 rubs.
  • composition may further contain at least one fragrance, at least one colorant.
  • a substantially anhydrous composition comprising about 0 - 80 % of at ieast one of a volatile organic solvent with an atmospheric boiling point of about 55 - 80oC, about 5-15% of a di-basic ester; and about 5 - 15% of at least one of a volatile organic solvent with atmospheric boiling point > 240oC.
  • compositions may be applied to a natural nail or a synthetic nail.
  • the natural nail is the natural keratinous material known as fingernails and toenails.
  • Synthetic nails are comprised of chemically reactive monomers, and/or oligomers, in combination with reactive or non-reactive polymers to create systems which are typically 100% solids and do not require non-reactive solvents, Upon pre-mixlng and subsequent application to the natural nail, or application and exposure to UV radiation, a chemical reaction ensues resulting in the formation of a long lasting, highly durable cross-linked nail coating that Is difficult to remove. Artificial nails may possess greatly enhanced adhesion, durability, as well as scratch and solvent resistance when compared to nail polishes.
  • Nail coatings have traditionally boon be classified into two categories; nail polishes; also known as lacquers, varnish or enamels and artificial nails; also known as gels or acrylics.
  • Nail polishes typically comprise various solid components which are dissolved and/of suspended in non- reactive solvents. Upon application and drying, the solids deposit on the nail surface as a clear, translucent or colored film.
  • Contemporary nail coatings are enhanced nail coatings contain higher performance polymers, higher levels of pigments, alternative pigments (e.g. blues and blacks ⁇ ., glitters, and photo-reactive nail coatings to provide a durable scratch resistant nail coating with improved adhesion.
  • alternative pigments e.g. blues and blacks ⁇ ., glitters
  • photo-reactive nail coatings to provide a durable scratch resistant nail coating with improved adhesion.
  • the expression "at least one” means one or more and thus includes Individual components as well as mixtures and combinations.
  • compositions and methods of the present disclosure consist of, or consist essentially of the elements and limitations described herein, as well as any additional or optional ingredients, components, or limitations otherwise useful as found in persona! care compositions intended for application to naif coatings.
  • a person skilled in the art will take care to select the optional additional additives and/or the amount thereof such that the advantageous properties of the composition according to the invention are not, or are not substantially, adversely affected by the envisaged addition, These substances may be selected variously by the person skitled In the art in order to prepare a composition which has the desired properties, for example, consistency or texture.
  • additives may be present in the composition In a proportion from 0% to :993 ⁇ 4 (such as from 0.01 % to 90%) relative to the total weight of the composition and further such as from 0.1 % to 50% (if present).
  • Non-llmitlng examples of additives include colors and fragrances.
  • Suitable colors are created by including in the composition, but are not limited to, pigments and dyes.
  • layers of composition describe the application of nail coatings.
  • a composition is painted on the nail to provide a cosmetic coloring or a healing or strengthening of the nail.
  • Application is done by painting a composition on the nail,
  • the nail coating composition fs applied, and at least partially dried as three, distinct layers.
  • application of any one Of the layers may be omitted.
  • application of any two of the layers may be omitted.
  • only a formulation for a color layer comprises colorant agents.
  • a formulation for any of the layers may comprise colorant
  • the organic solvent is readily volatile at room temperature. Upon application, the solvent readily volatilizes leaving regions of Increased porosity throughout the nail coating, These porous regions later facilitate' the entry of a remover solvent which may be acetone,
  • Non limiting examples of suitable Solvents include ethyl acetate, methyl acetate, and acetone.
  • Table 1 compares combinations of a volatile organic solvent with an atmospheric boiling point of about 55 - 80oC, at least one of a volatile organic solvent with atmospheric boiling point > 240oC, and at least one of a di-basic ester. Each experimental sample was prepared and evaluated as follows:

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  • 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

The present disclosure relates generally to a composition comprising a substantially anhydrous composition comprising at least one of a volatile organic solvent with an atmospheric boiling point of about 55 - 80°C at least one of a volatile organic solvent with atmospheric boiling point > 240°C, and at feast one of a di-basic ester.

Description

NAIL COATING REMOVER
This application claims priority from co-pending provisional application Serial Number 62/429,455, filed December 2, 2016, the entire disclosure of which is hereby incorporated by reference.
FIELD
[0001] The present disclosure relates generally to a composition for nail coating remover, and particularly, but .not by way of limitation, a combination of ingredients that improve removal of difficult enamels and glitters used in nail coating on the naii.
BACKGROUND f0002J The information provided below is not admitted to be prior art to the present invention, but Is provided solely to assist the understanding of the reader.
£0003] Contemporary nail coatings use higher performance polymers, higher levels of pigments, alternative pigments (e.g. blues and blacks); glitters, and photo-reactive nail coatings to provide a durable scratch resistant nail coating with improved adhesion. These contemporary nail coatings are longer lasting and difficult to remove with the traditional nail coating removers currently on the market.
[0004] There is a need to develop a nail coating remover that quickly and completely removes contemporary nail coatings.
SUMMARY
[0005] in ah embodiment a composition that is substantially anhydrous composition comprises at least one of a volatile organic solvent with an atmospheric boiling point of about 55 ~ 80ºC, at least one of a volatile organic solvent with atmospheric boiling point > 240'C, and at least one of a di-basic ester. The volatile organic solvent with an atmospheric boiling point of about 55 - 80ºC Is an acetone or acetate. Non-llmttlng examples of the acetate .is ethyl acetate or methyl acetate. A non-iimiting example of the volatile organic solvent with atmospheric boiling point > 240ºC is propylene carbonate. A non-limiting example of the dibasic ester is diethylhexyl maieate. [0006] In an embodiment the composition disclosed Is applied to a dried nail coating on natural or synthetic nails.
[0007] In an embodiment the composition when applied, to a dried nati poating on natural or synthetic nails removes the nail coating with < 12 rubs.
[0008] In an embodiment the composition may further contain at least one fragrance, at least one colorant.
[0009] In an embodiment disclosed is a substantially anhydrous composition comprising about 0 - 80 % of at ieast one of a volatile organic solvent with an atmospheric boiling point of about 55 - 80ºC, about 5-15% of a di-basic ester; and about 5 - 15% of at least one of a volatile organic solvent with atmospheric boiling point > 240ºC.
DESCRIPTION
[0010] Embodiments of the present invention are discussed in detail below. In describing embodiments, specific terminology is employed for the sake of clarity. However, the invention is not Intended to be limited to the specific terminology so selected. While specific exemplary embodiments are discussed, It should be understood that this is done for illustration purposes only, A person skilled in the relevant art will recognize that other components and configurations can be used without parting from the spirit and scope of the invention. While a number of embodiments and features are described herein, it is to be understood that the various features of the Invention and aspects of embodiments, even if described separately, may be combined unless mutually exclusive or contrary to the specific description. All references cited herein are incorporated by reference as if each had been individually incorporated.
[0011] As used In the present disclosure the compositions may be applied to a natural nail or a synthetic nail. The natural nail is the natural keratinous material known as fingernails and toenails. Synthetic nails are comprised of chemically reactive monomers, and/or oligomers, in combination with reactive or non-reactive polymers to create systems which are typically 100% solids and do not require non-reactive solvents, Upon pre-mixlng and subsequent application to the natural nail, or application and exposure to UV radiation, a chemical reaction ensues resulting in the formation of a long lasting, highly durable cross-linked nail coating that Is difficult to remove. Artificial nails may possess greatly enhanced adhesion, durability, as well as scratch and solvent resistance when compared to nail polishes.
[0012] Nail coatings have traditionally boon be classified into two categories; nail polishes; also known as lacquers, varnish or enamels and artificial nails; also known as gels or acrylics. Nail polishes typically comprise various solid components which are dissolved and/of suspended in non- reactive solvents. Upon application and drying, the solids deposit on the nail surface as a clear, translucent or colored film.
[0013] Contemporary nail coatings are enhanced nail coatings contain higher performance polymers, higher levels of pigments, alternative pigments (e.g. blues and blacks}., glitters, and photo-reactive nail coatings to provide a durable scratch resistant nail coating with improved adhesion.
[0014] As used herein, the expression "at least one" means one or more and thus includes Individual components as well as mixtures and combinations.
[0015] AS' used herein, the expression "about" shall generally mean within 5 percent of a given value or range. Other than in the operating examples, or where otherwise indicated, all numbers expressing quantities of Ingredients andfor reaction conditions are to be understood as being modified in all instances by the term "about".
10016] The cosmetic compositions and methods of the present disclosure consist of, or consist essentially of the elements and limitations described herein, as well as any additional or optional ingredients, components, or limitations otherwise useful as found in persona! care compositions intended for application to naif coatings. A person skilled in the art will take care to select the optional additional additives and/or the amount thereof such that the advantageous properties of the composition according to the invention are not, or are not substantially, adversely affected by the envisaged addition, These substances may be selected variously by the person skitled In the art in order to prepare a composition which has the desired properties, for example, consistency or texture. These additives may be present in the composition In a proportion from 0% to :99¾ (such as from 0.01 % to 90%) relative to the total weight of the composition and further such as from 0.1 % to 50% (if present). Non-llmitlng examples of additives include colors and fragrances.
[0017] Suitable colors are created by including in the composition, but are not limited to, pigments and dyes.
[0018] According to the present disclosure .layers of composition describe the application of nail coatings. A composition is painted on the nail to provide a cosmetic coloring or a healing or strengthening of the nail. Application is done by painting a composition on the nail, According to an aspect, the nail coating composition fs applied, and at least partially dried as three, distinct layers. According to an aspect, application of any one Of the layers may be omitted. According to an aspect, application of any two of the layers may be omitted. According to an aspect, only a formulation for a color layer comprises colorant agents. According to an aspect, a formulation for any of the layers may comprise colorant
[0019] The organic solvent is readily volatile at room temperature. Upon application, the solvent readily volatilizes leaving regions of Increased porosity throughout the nail coating, These porous regions later facilitate' the entry of a remover solvent which may be acetone,
[0020] Non limiting examples of suitable Solvents include ethyl acetate, methyl acetate, and acetone.
EXAMPLE
[0021] Table 1 compares combinations of a volatile organic solvent with an atmospheric boiling point of about 55 - 80ºC, at least one of a volatile organic solvent with atmospheric boiling point > 240ºC, and at least one of a di-basic ester. Each experimental sample was prepared and evaluated as follows:
Figure imgf000006_0001
Table 1 : High Efficiency Nail Coating Remover Formulations (Acetone Baaed)
Note: Three (3) commercial nail coatortg remover products were used as controls in this study:
• Cutex Quick & Gentle Nail Enamel Remover-Regular: 23 rubs
• Cutex Nail Enamel Remover-Humectante: 23 rubs
• Cutex Non-Acetone Nail Enamel Remover. 27 rubs
Table 2: High Efficiency Nail Coating Remover Formulations (Methyl Acetate-Based)
Figure imgf000007_0001
Note: Three (3) commercial nail coating remover products were used as controls in this study;
• Cutex Quick & Gentle Nail Enamel Remover-Regular: 23 rubs
• Cutex Nail Enamel Remover-Humactante: 23 rubs
• Cutex Non-Aceione Nail Enamel Remover. 27 rubs
Table 3: High Efficiency Nail Coating Remover Formulations (Ethyl Acetate-Based)
Figure imgf000008_0001
Note: Three (3) commercial nail coating remover products were used as controis in this study:
Cutex Quick & Gentle Nail Enamel Remover-Regular. 23 rubs
• Cutex Nail Enamel Remover-Humectante: 23 rubs
• Cutex Non-Acetone Nail Enamel Remover. 27 rubs
[0022] Raw ingredients were weighed Into clean 100-ml. sealable glass jars and were mixed thoroughly using a Red Devil Model 1400 Paint Conditioner for 5 minutes.
[00023]To demonstrate enhanced removal efficacy as a result of multiple raw ingredient synergies in the 18 experimental formulas tested herefn, the removal efficacy of each "neat" solvent (i.e.100% acetone, 100% ethyl acetate, 100% methyl acetate and 100% 100% propylene carbonate) also was behchmarked in this study.
[0024] TESTING METHODOLOGY:
[0025] To create a suitable test substrate for quantitative evaluation of removal efficacy, a series of drawdowns were cast onto clean glass panels using a Bird Film Applicator of 6 mil wet film thickness (Model # AP-3xOQ6SS; Paul N, Gardner & Co.) The test laoquer formula used in this study was Sinful Colors Nail Enamel Bahgin' Blue. This is a medium blue "glitter" shade containing 4.98% polyethylene terephthalate effects' pigments. This particular shade, is representative of a contemporary nail coating formu!ation that would be highty tenacious to users' nails and therefore would be quite difficult to remove completely after many days of wear. All drawdowns' were allowed to dry at ambient temperature (approximately 25 deg. C.) for at least 15 days before testing.
[0026) To provide a quantitative measurement of the relative removal efficacy of each experimental formula or control product evaluated herein, a clean cotton bait was saturated with the disclosed compositions then pressed gently onto the surface of the dried nail coating described above. The wet cotton ball then was rubbed in a clockwise motion within a circular test area approximately in diameter. The number of rubs needed to completely dissolve the
Figure imgf000009_0001
nail coating to bare glass was recorded for each test sample.
[0027] Table 1 : High Efficiency Nail Lacquer Remover Formulations (Acetone Based)
[0028] Table 2: High Efficiency Nail Lacquer Remover Formulations (Methyl Acetate-Based)
[0029] Table 3: High Efficiency Nail Lacquer Remover Formulations (Ethyl Acetate-Based)

Claims

CLAIMS What is claimed is:
1. A substantially anhydrous composition comprising at least one of a volatile organic solvent with an atmosphere boiling point of about 55 - 80ºC. at least one of a volatile organic solvent with atmospheric boiling point > 240°C, and at least one of a dl-basic ester.
2. The composition of claim 1 , wherein, the volatile organic solvent with an atmospheric boiling point of about 55 - 80ºC" is an acetone or an acetate.
3. The composition of claim 2, wherein the acetate is ethyl acetate.
4. The composition of claim 2, wherein the acetate is a methyl acetate,
5. The composition of claim 1 , wherein the volatile organic solvent with atmospheric boiling point > '240°C Is propylene carbonate,
6. The composition of claim 1 , wherein the di-basic ester is diethylhexyl mateate.
7. The composition of claim 1 , wherein the composition fs applied to a dried nail coating on natural or synthetic nails.
8. The composition of claim 2, wherein the composition when applied to a dried naii coating on natural or synthetic nails removes the nail coating with < 12 rubs.
9. The composition of claim 1 wherein said composition may further comprise at least one
fragrance.
10. The composition of claim 1 , wherein said composition may further comprise at least one colorant.
11. A substantial anhydrous composition comprising about 0 - 80 % of at least one of a volatile organic solvent with an atmospheric boiling point of about 55 - 80ºC, about 5-15% of a di-basic ester; and about 5 - 15% of at least one of a volatile organic solvent with atmospheric boiling point > 240ºC.
12. The composition of claim 1 , wherein, the volatile organic solvent with an atmospheric boiling point of about 55 - 80ºC is an acetone or an acetate.
13. The composition of claim 2, wherein the acetate is ethyl acetate.
14. The composition of claim 2, wherein the acetate is a methyl acetate.
15. The composition of claim 1 , wherein the volatile organic solvent with atmqspheric boiling point > 240ºC is propylene carbonate.
16. The composition of claim 1 , wherein the di-basic ester is diethyihexyl ma!eate,
17. The composition of claim 1 , wherein the composition is applied to a dried nail coating on natural or synthetic nails.
16. The composition of claim 2, wherein the composition when applied to a dried nail coating on natural or synthetic nails removes the nail coating with < 12 rubs.
19. The composition of claim 1 wherein said composition may further comprise at least one fragrance.
20. The composition of claim 1 , wherein said composition may further comprise at least one colorant.
PCT/US2017/062748 2016-12-02 2017-11-21 Nail coating remover WO2018102195A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662429455P 2016-12-02 2016-12-02
US62/429,455 2016-12-02

Publications (1)

Publication Number Publication Date
WO2018102195A1 true WO2018102195A1 (en) 2018-06-07

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Country Link
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5007969A (en) * 1988-05-20 1991-04-16 The Boeing Company Low toxicity liquid solvent
US5486305A (en) * 1994-09-19 1996-01-23 Chesebrough-Pond's Usa Co. Nail polish remover
US20050202982A1 (en) * 2004-03-15 2005-09-15 Daniel Perlman pH-buffered alkylene carbonate nail polish and paint remover
US7074392B1 (en) * 2000-03-27 2006-07-11 Taro Pharmaceutical Industries Limited Controllled delivery system of antifungal and keratolytic agents for local treatment of fungal infections
US20120315229A1 (en) * 2011-06-09 2012-12-13 Momentive Performance Materials Inc. Clarifying agents for organomodified silicones

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5007969A (en) * 1988-05-20 1991-04-16 The Boeing Company Low toxicity liquid solvent
US5486305A (en) * 1994-09-19 1996-01-23 Chesebrough-Pond's Usa Co. Nail polish remover
US7074392B1 (en) * 2000-03-27 2006-07-11 Taro Pharmaceutical Industries Limited Controllled delivery system of antifungal and keratolytic agents for local treatment of fungal infections
US20050202982A1 (en) * 2004-03-15 2005-09-15 Daniel Perlman pH-buffered alkylene carbonate nail polish and paint remover
US20120315229A1 (en) * 2011-06-09 2012-12-13 Momentive Performance Materials Inc. Clarifying agents for organomodified silicones

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