FR2556960A1 - COMPOSITION BASED ON ACRYLIC CARBOXILIC RESINS FOR EMBELLISHING AND MAINTAINING HAIR - Google Patents
COMPOSITION BASED ON ACRYLIC CARBOXILIC RESINS FOR EMBELLISHING AND MAINTAINING HAIR Download PDFInfo
- Publication number
- FR2556960A1 FR2556960A1 FR8320629A FR8320629A FR2556960A1 FR 2556960 A1 FR2556960 A1 FR 2556960A1 FR 8320629 A FR8320629 A FR 8320629A FR 8320629 A FR8320629 A FR 8320629A FR 2556960 A1 FR2556960 A1 FR 2556960A1
- Authority
- FR
- France
- Prior art keywords
- resin
- compositions according
- acrylic
- perfume
- castor oil
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions 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
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
Abstract
COMPOSITIONS POUR L'EMBELLISSEMENT ET LE MAINTIEN DE LA CHEVELURE, CARACTERISEES EN CE QU'ELLES CONTIENNENT COMME CONSTITUANT ACTIF ESSENTIEL UNE RESINE DE TYPE CARBOXYLIQUE D'ORIGINE ACRYLIQUE NEUTRALISEE PAR UN AGENT ALCALIN.COMPOSITIONS FOR THE EMBELLISHMENT AND MAINTENANCE OF THE HAIR, CHARACTERIZED IN THAT THE ESSENTIAL ACTIVE CONSTITUENT CONTAINS A CARBOXYL TYPE RESIN OF ACRYLIC ORIGIN NEUTRALIZED BY AN ALKALINE AGENT.
Description
La présente invention concerne de nouvelles compositions cosmétiquesThe present invention relates to new cosmetic compositions
destinées au traitement de la chevelure, notamment pour en assurer le maintien, mais également pour en améliorer la intended for the treatment of the hair, in particular to ensure the maintenance of it, but also to improve the
conservation, et la rendre plus attrayante. conservation, and make it more attractive.
Ces nouvelles compositions se caractérisent par la présence simultanée d'une part d'une résine de type carboxylique These new compositions are characterized by the simultaneous presence on the one hand of a resin of the carboxylic type.
d'origine acrylique, et de préférence résultant de la copolymé- of acrylic origin, and preferably resulting from the copolymer-
risation de l'acide acrylique avec l'éther allylique du sucrose, rization of acrylic acid with the allyl ether of sucrose,
et d'autre part d'un agent alcalin neutralisant pour cette ré- and on the other hand an alkaline neutralizing agent for this re-
sine, en provoquant ainsi sa gélification, tout en lui conservant sine, thus causing its gelation, while preserving it
sa transparence.its transparency.
Il convient de noter que depuis fort longtemps on a tenté de proposer des gels d'origine diverses pour embellir et maintenir la chevelure. Toutefois aucun de ces gels n'a jamais donné totalement satisfaction, car, ou bien ils laissaient les cheveux poisseux ou gras, ou bien ils se résorbaient en créant It should be noted that for a long time we have tried to offer gels of various origins to beautify and maintain the hair. However, none of these gels has ever been completely satisfactory, because either they left the hair sticky or oily, or they were absorbed by creating
dans la chevelure une poussière difficile à éliminer. dust in the hair which is difficult to remove.
Au contraire, pour la première fois, les compositions définies ci-dessus présentent l'avantage de se travailler sans On the contrary, for the first time, the compositions defined above have the advantage of being worked without
poisser ni graisser les cheveux et sans y laisser de poussière. pitch or grease the hair and leave no dust on it.
La mise en oeuvre de l'invention peut se concevoir de The implementation of the invention can be conceived of
diverses façons, selon l'usage qui doit être fait de la compo- various ways, depending on the use to be made of the compound
sition. Selon un premier mode de réalisation, la composition a sition. According to a first embodiment, the composition has
entre autres pour but de maintenir la chevelure, tout en la lais- among other things to maintain the hair, while leaving it
sant souple et fluide, et dans ce cas la composition peut conte- flexible and fluid, and in this case the composition may contain
nir un agent humectant, choisi de préférence parmi les alcools, provide a humectant, preferably chosen from alcohols,
tels que notamment les polyols.such as in particular polyols.
Selon un second mode de réalisation, la composition a entres autres pour but de fixer la chevelure, à un degré plus ou moins important de rigidité, et elle comporte au surplus à cet effet une autre résine synthétique, de préférence un polymère Qu According to a second embodiment, the composition has, among other things, the purpose of fixing the hair, to a greater or lesser degree of rigidity, and it also comprises for this purpose another synthetic resin, preferably a polymer Qu
un copolymêre de la vinylpyrolidone. a vinylpyrolidone copolymer.
Dans tous les cas, la composition contient, en addition In all cases, the composition contains, in addition
des agents en assurant la conservation et la rendant plus attra- agents ensuring conservation and making it more attractive
yante pour le consommateur, tels que colorants, parfums, pigments, for the consumer, such as dyes, perfumes, pigments,
paillettes et analogues.glitter and the like.
La résine qui représente, avec son agent neutralisant, le constituant essentiel des compositions selon l'invention, et The resin which, with its neutralizing agent, represents the essential constituent of the compositions according to the invention, and
plus spécialement le produit de copolymérisation (ou de réticu- more especially the product of copolymerization (or of reticu-
2 25569602 2556960
lation) de l'acide acrylique avec l'éther allylique du sucrose est présente dans ces compositions à raison d'environ 0,1 à 2 Z. On peut par exemple utiliser à cet effet le produit commercialisé sous la marque CARBOMER 940 ou CARBOPOL 940 par la firme Goodrich lation) of acrylic acid with the allyl ether of sucrose is present in these compositions in an amount of approximately 0.1 to 2%. The product sold under the brand CARBOMER 940 or CARBOPOL 940 can for example be used for this purpose. by the firm Goodrich
(USA).(USA).
Comme agent neutralisant de cette résine, et représen- As a neutralizing agent for this resin, and represents
tant donc également un constituant essentiel des compositions selon l'invention, on peut utiliser pratiquement n'importe quel composé alcalin minéral, tel que Na OH, K OH, NH40H, le borax, therefore also being an essential constituent of the compositions according to the invention, practically any mineral alkaline compound can be used, such as Na OH, K OH, NH40H, borax,
et analogues, ou organique, tel que les amines, simples ou sub- and the like, or organic, such as amines, simple or sub-
stitués, par exemple la mono-, la di- et la tri-éthanolamine, l'isopropylamine, l'éthylhexylamine, la triéthylénamine, la substances, for example mono-, di- and tri-ethanolamine, isopropylamine, ethylhexylamine, triethylenamine,
triamylamine, et analogues. Cet agent est présent dans ces com- triamylamine, and the like. This agent is present in these com-
positions en quantité suffisante pour neutraliser la résine, partiellement ou totalement ou même en léger excès, à savoir positions in sufficient quantity to neutralize the resin, partially or totally or even in slight excess, namely
de 0,1 à 3 %.0.1 to 3%.
Pour préparer les compositions selon l'invention, on prépare séparément, d'une part une suspension aqueuse de la résine, à laquelle il convient d'ajouter un agent conservateur, qui doit bien entendu être compatible avec les autres constituants, et d'autre part une solution aqueuse de l'agent neutralisant avec les autres agents additionnels. Le simple mélange de la suspension avec la solution provoque la formation instantanée To prepare the compositions according to the invention, an aqueous suspension of the resin is prepared separately, to which a preservative should be added, which must of course be compatible with the other constituents, and on the other hand apart from an aqueous solution of the neutralizing agent with the other additional agents. Simple mixing of the suspension with the solution causes instant formation
du gel qui, est immédiatement utilisable. gel which is immediately usable.
Dans le second mode de réalisation de l'invention, la composition contient une certaine proportion d'une seconde résine du type polyvinylpyrrolidone, jouant le r8le d'agent fixant. Dans ce cas, la nature et la proportion de cet agent seront proportionnels au degré de rigidité que l'on souhaite conférer à la coiffure. La proportion ne devra cependant pas dépasser environ 20 %. Comme copolymères de la polyvinylpyrrolidone, on pourra utiliser par exemple des copolymêres avec le méthacrylate de diméthylaminoéthyle commercialisés sous les marques AGENT In the second embodiment of the invention, the composition contains a certain proportion of a second resin of the polyvinylpyrrolidone type, playing the role of fixing agent. In this case, the nature and the proportion of this agent will be proportional to the degree of rigidity which it is desired to impart to the hairstyle. The proportion should not, however, exceed around 20%. As polyvinylpyrrolidone copolymers, it is possible, for example, to use copolymers with dimethylaminoethyl methacrylate sold under the brands AGENT
AT-858, AGENT AT-937 et COPOLYMER 845 par GAF Corp.(USA). AT-858, AGENT AT-937 and COPOLYMER 845 by GAF Corp. (USA).
Ainsi, par exemple, environ 3 % de polyvinylpyrolidone ajoutés à un gel tel qu'obtenu comme indiqué ci-dessus conduisent à une Thus, for example, approximately 3% of polyvinylpyrolidone added to a gel as obtained as indicated above lead to a
composition qui, outre les effets propres du gel sur la cheve- composition which, in addition to the proper effects of the gel on the hair
lure et ceux de la résine, garantissent la fixation de la coif- lure and those of the resin, guarantee the fixing of the coif-
fure, fixation qui peut être légère ou très accentuée suivant la fure, fixation which can be light or very accentuated depending on the
nature et la dose d'agent fixant utilisé. nature and dose of fixing agent used.
3 25569603 2556960
Enfin, comme indiqué précédemment, des agents addi- Finally, as indicated above, additive agents
tionnels pourront également être ajoutés aux compositions selon can also be added to the compositions according to
l'invention, soit pour en assurer la stabilité et la conserva- the invention, either to ensure its stability and conservation
tion, par exemple des composés séquestrants pour le calcium tels que le sel de sodium de l'acide éthylène-diamine-têtra- acétique (EDTA), commercialisé notamment sous la marque TRILON B, soit pour les rendre plus attrayantes, par exemple par des tion, for example calcium sequestering compounds such as the sodium salt of ethylene diamine-tetraacetic acid (EDTA), marketed in particular under the brand TRILON B, or to make them more attractive, for example by
colorants ou des parfums appropriés. dyes or suitable fragrances.
Les exemples suivants, donnés au titre d'illustration et sans aucun caracètre limitatif, se réfèrent à trois modes de The following examples, given by way of illustration and without any limiting character, refer to three modes of
réalisation typiques des compositions selon l'invention. typical production of the compositions according to the invention.
Exemple 1: Composition non fixante.Example 1: Non-fixing composition.
Les constituants de cette composition sont les sui- The constituents of this composition are the following:
vants (en % en poids).(in% by weight).
CARBOPOL 940 0,80CARBOPOL 940 0.80
Triéthanolamine 0,84 Glycérine (humectant) 0,50 Chloracétamide + Benzoate de sodium (agent conservateur) 0,30 Triethanolamine 0.84 Glycerin (humectant) 0.50 Chloracetamide + Sodium benzoate (preservative) 0.30
TRILON B 0,10TRILON B 0.10
Huile de ricin hydrogénée et polyoxyéthylènée (solubilisant pour le parfum) 0,15 Hydrogenated and polyoxyethylene castor oil (solubilizer for perfume) 0.15
Glycérides capriques et capry-Capric and capry glycerides
liques polyoxyéthylénés (solu-polyoxyethylenated liquids (solu-
bilisants) 0,15 Parfum 0,10bilisants) 0.15 Perfume 0.10
Colorant 0,33.Dye 0.33.
Le reste (complément à 100 %) de la composition est constitué par l'eau utilisée dans la préparation, comme indiqué The rest (100% complement) of the composition consists of the water used in the preparation, as indicated
plus haut.upper.
Il convient de noter que l'huile de ricin hydrogénée et polyoxyéthylénée utilisée comme agant de solubilisation du It should be noted that the hydrogenated and polyoxyethylenated castor oil used as a solubilizing agent for
parfum contribue également à la texture agréable de la composi- fragrance also contributes to the pleasant texture of the composition
tion.tion.
Cette composition ne joue pas de rôle fixateur, mais a un effet embellissant et assouplissant sur la chevelure dont This composition does not play a fixing role, but has an embellishing and softening effect on the hair,
elle contribue au maintien.it contributes to maintenance.
Les deux autres compositions, par contre, fixent la chevelure en séchant: Exemple 2: Composition légèrement fixante (en % en poids) The other two compositions, on the other hand, fix the hair by drying: Example 2: Slightly fixing composition (in% by weight)
CARBOPOL 940 0,80CARBOPOL 940 0.80
Triethanolamine 0,96 Chloracetamide + Benzoate de sodium 0,30 TRILON B poudre 0,10 Polyvinylpyrrolidone 2,80 Huile de ricin hydrogénée :0 polyoxyethylènae 0,15 Triethanolamine 0.96 Chloracetamide + Sodium benzoate 0.30 TRILON B powder 0.10 Polyvinylpyrrolidone 2.80 Castor oil, hydrogenated: 0 polyoxyethylenea 0.15
Glycérides capriques et capry-Capric and capry glycerides
liques polyoxyethylènés 0,15 Parfum 0,10 Colorants 0,35 Eau q.s. 100 polyoxyethylated liquids 0.15 Perfume 0.10 Dyes 0.35 Water q.s. 100
Exemple 3: Composition fortement fixante (% en poids). Example 3: Strongly fixing composition (% by weight).
CARBOPOL 940 1,00CARBOPOL 940 1.00
Triethanolamine 1,60 Propylèneglycol 2,00 Chloracetamide + Benzoate de sodium 0,30 Triethanolamine 1.60 Propylene glycol 2.00 Chloracetamide + Sodium benzoate 0.30
TRILON B 0,10TRILON B 0.10
COPOLYMER 845 15,00COPOLYMER 845 15.00
Huile de ricin hydrogénée polyoxyethylènge 0,15 Glycérides capriques et capryliques polyoxyethylènée 0,15 Parfum 0,10 Colorants 0,60 Eau q.s. 100 Bien entendu l'invention n'est pas limitée aux exemples de compositions et de constituants précis de ces compositions énumérées ci-dessus, notamment en ce qui concerne les produits Polyoxyethylene hydrogenated castor oil 0.15 Polyoxyethylenic caprylic and caprylic glycerides 0.15 Perfume 0.10 Dyes 0.60 Water q.s. 100 Of course the invention is not limited to the examples of precise compositions and constituents of these compositions listed above, in particular with regard to the products
identifiés par leurs marques commerciales et les agents addi- identified by their trademarks and the addi-
tionnels, et tout constituant équivalent à l'un ou l'autre ren- and any constituent equivalent to one or the other
trera dans le cadre de l'invention.will be within the scope of the invention.
25569602556960
Claims (11)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8320629A FR2556960B1 (en) | 1983-12-21 | 1983-12-21 | COMPOSITION BASED ON ACRYLIC CARBOXILIC RESINS FOR EMBELLISHING AND MAINTAINING HAIR |
LU85674A LU85674A1 (en) | 1983-12-21 | 1984-12-07 | COMPOSITIONS FOR THE TREATMENT OF HAIR |
GB08431673A GB2153375A (en) | 1983-12-21 | 1984-12-14 | Hair treatment compositions |
DE19843446024 DE3446024A1 (en) | 1983-12-21 | 1984-12-18 | HAIR CARE PRODUCTS |
ES538870A ES8600925A1 (en) | 1983-12-21 | 1984-12-20 | Hair treatment compositions |
BE6/48050A BE901340A (en) | 1983-12-21 | 1984-12-20 | COMPOSITIONS FOR THE TREATMENT OF HAIR. |
CH6067/84A CH664082A5 (en) | 1983-12-21 | 1984-12-20 | COMPOSITIONS FOR THE TREATMENT OF HAIR. |
NL8403914A NL8403914A (en) | 1983-12-21 | 1984-12-21 | COMPOSITIONS FOR THE DECORATION AND MAINTENANCE OF THE HAIRCARE. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8320629A FR2556960B1 (en) | 1983-12-21 | 1983-12-21 | COMPOSITION BASED ON ACRYLIC CARBOXILIC RESINS FOR EMBELLISHING AND MAINTAINING HAIR |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2556960A1 true FR2556960A1 (en) | 1985-06-28 |
FR2556960B1 FR2556960B1 (en) | 1990-01-19 |
Family
ID=9295472
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR8320629A Expired - Fee Related FR2556960B1 (en) | 1983-12-21 | 1983-12-21 | COMPOSITION BASED ON ACRYLIC CARBOXILIC RESINS FOR EMBELLISHING AND MAINTAINING HAIR |
Country Status (8)
Country | Link |
---|---|
BE (1) | BE901340A (en) |
CH (1) | CH664082A5 (en) |
DE (1) | DE3446024A1 (en) |
ES (1) | ES8600925A1 (en) |
FR (1) | FR2556960B1 (en) |
GB (1) | GB2153375A (en) |
LU (1) | LU85674A1 (en) |
NL (1) | NL8403914A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1318733A (en) * | 1962-01-10 | 1963-02-22 | Garnier Lab | New cosmetic composition |
FR1343194A (en) * | 1962-12-15 | 1963-11-15 | Wuertt Parfuemerie | Cosmetic product in the form of jelly |
FR2393573A1 (en) * | 1977-06-10 | 1979-01-05 | Gaf Corp | HAIR PREPARATIONS CONTAINING A VINYLPYRROLIDONE COPOLYMER |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB626626A (en) * | 1944-10-25 | 1949-07-19 | Gen Aniline & Film Corp | Reversible gel composition and method of preparation |
GB747806A (en) * | 1953-03-27 | 1956-04-11 | Gen Aniline & Film Corp | Hair waving and setting composition |
US3171784A (en) * | 1956-11-09 | 1965-03-02 | Gen Aniline & Film Corp | Copolymer of vinyl pyrrolidone and vinyl acetate as aerosol hair spray |
GB858430A (en) * | 1958-02-10 | 1961-01-11 | Ashe Chemical Ltd | Preparations for the treatment of the hair |
GB993967A (en) * | 1961-01-23 | 1965-06-02 | Superma Ltd | Hair treatment |
GB1146155A (en) * | 1965-03-26 | 1969-03-19 | Mitsubishi Rayon Co | Hair lacquers |
JPS4829137B1 (en) * | 1968-07-10 | 1973-09-07 | ||
LU58617A1 (en) * | 1969-05-09 | 1971-03-09 | ||
US3869546A (en) * | 1972-12-22 | 1975-03-04 | Cutter Lab | Adjuvant compositions and medicinal mixtures comprising them |
DE2404793A1 (en) * | 1974-02-01 | 1975-08-14 | Basf Ag | USE OF MIXED POLYMERISATES BASED ON HALF-ESTABLISHED DICARBONIC ACIDS AS EFFECTIVE COMPONENTS IN HAIR CARE PRODUCTS |
US4237253A (en) * | 1977-04-21 | 1980-12-02 | L'oreal | Copolymers, their process of preparation, and cosmetic compounds containing them |
US4192861A (en) * | 1978-05-05 | 1980-03-11 | National Starch And Chemical Corporation | Hydrocarbon propelled aerosol hair spray compositions |
-
1983
- 1983-12-21 FR FR8320629A patent/FR2556960B1/en not_active Expired - Fee Related
-
1984
- 1984-12-07 LU LU85674A patent/LU85674A1/en unknown
- 1984-12-14 GB GB08431673A patent/GB2153375A/en not_active Withdrawn
- 1984-12-18 DE DE19843446024 patent/DE3446024A1/en not_active Withdrawn
- 1984-12-20 ES ES538870A patent/ES8600925A1/en not_active Expired
- 1984-12-20 BE BE6/48050A patent/BE901340A/en not_active IP Right Cessation
- 1984-12-20 CH CH6067/84A patent/CH664082A5/en not_active IP Right Cessation
- 1984-12-21 NL NL8403914A patent/NL8403914A/en not_active Application Discontinuation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1318733A (en) * | 1962-01-10 | 1963-02-22 | Garnier Lab | New cosmetic composition |
FR1343194A (en) * | 1962-12-15 | 1963-11-15 | Wuertt Parfuemerie | Cosmetic product in the form of jelly |
FR2393573A1 (en) * | 1977-06-10 | 1979-01-05 | Gaf Corp | HAIR PREPARATIONS CONTAINING A VINYLPYRROLIDONE COPOLYMER |
Non-Patent Citations (1)
Title |
---|
R.A.K. RIECHSTOFFE, AROMEN, KOSMETICA, vol. 29, no. 10, octobre 1979, St. Peter-Ording (DE) * |
Also Published As
Publication number | Publication date |
---|---|
FR2556960B1 (en) | 1990-01-19 |
ES538870A0 (en) | 1985-11-01 |
DE3446024A1 (en) | 1985-07-04 |
LU85674A1 (en) | 1985-07-24 |
BE901340A (en) | 1985-04-16 |
GB8431673D0 (en) | 1985-01-30 |
GB2153375A (en) | 1985-08-21 |
NL8403914A (en) | 1985-07-16 |
ES8600925A1 (en) | 1985-11-01 |
CH664082A5 (en) | 1988-02-15 |
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