EP3125862A1

EP3125862A1 - Cosmetic preparation for uv-protection based on acrylate

Info

Publication number: EP3125862A1
Application number: EP15711164.2A
Authority: EP
Inventors: Andreas Bleckmann; Heike Lerg; David SCHLENKER
Original assignee: Beiersdorf AG
Current assignee: Beiersdorf AG
Priority date: 2014-04-01
Filing date: 2015-03-20
Publication date: 2017-02-08
Also published as: DE102014206224A1; WO2015150115A1

Abstract

The invention relates to a cosmetic preparation containing a) an acrylate copolymer having a glass transition temperature of between -5 to -15 C°, measured by means of DSC and b) water-soluble UV filter.

Description

description

COSMETIC PREPARATION FOR UV-PROTECTION ACRYLATE-BASED

The present invention relates to a cosmetic preparation comprising an acrylate copolymer having a glass transition temperature of -5 to -15 ° C, measured by means of DSC and water-soluble UV filters.

The trend away from the noble paleness to the "healthy, sporty brown skin" has been unbroken for years, to achieve this, people are putting their skin on the skin

Solar radiation, as this causes a pigmentation in the sense of melanin formation. However, the ultraviolet radiation of sunlight also has a damaging effect on the skin. In addition to the acute injury (sunburn), long-term damage such as an increased risk of developing skin cancer occurs due to excessive exposure to light from the UVB range (wavelength: 280-320 nm). The excessive action of the UVB and UVA radiation (wavelength: 320-400 nm) also leads to a weakening of the elastic and collagen fibers of the connective tissue. This leads to numerous phototoxic and photoallergic reactions and leads to premature skin aging.

To protect the skin, therefore, a number of sunscreen filter substances have been developed which can be used in cosmetic preparations. These UVA and UVB filters are in the form of positive lists in most industrialized countries such as Appendix 7 of the

Cosmetics Regulation summarized.

However, the variety of commercially available sunscreens must not obscure the fact that these prior art formulations have a number of disadvantages.

A relatively new product form for skin care are the hydrodispersions used under the shower, which are applied to the wet skin after a first showering process, with excess being left over in a second showering session, not on the skin Skin fixed preparation is rinsed off (so-called in-shower products, which are analogous to shower gel used, in contrast to these, however, do not cleanse, but apply the care product to the skin).

A disadvantage of the conventional in-shower products is the fact that they can hardly be effectively applied with UV light protection filters for the UV protection of the skin. Most of the UV filters are rinsed more or less completely from the skin during the second showering process, so that virtually no UV protection can occur.

It was therefore the object of the present invention to develop an in-shower product with which larger amounts of UV filters can be effectively applied to the skin.

In particular, SPFs of at least SPF 6 should be at a normal

Application can be achieved.

Surprisingly, the objects are achieved by a cosmetic preparation comprising a) an acrylate copolymer having a glass transition temperature of -5 to -15 ° C, measured by means of DSC and

b) water-soluble UV filters.

The solution of the problem is particularly surprising because the skilled person had to assume that water-soluble UV filters can be rinsed off particularly easily during in-shower application and show a particularly low adhesion to the skin.

The glass transition temperature according to the invention is determined by means of differential scanning calorimetry. In the context of the present invention (i.e.

according to the invention) was a Mettler DCS 1 device in the temperature cycle mode with a perforated aluminum crucible (40μΙ), at a measurement temperature of -50 ° C to +150 ° C, a heating rate of 10 ° C / min. and nitrogen used as purge gas (nitrogen 5.0).

Skin hydration is determined according to the invention by the following method:

First, in a 1. Measurement of skin hydration with the Corneometer C 825 (Courage & Khazaka) on 4 areas on the forearms. This value corresponds to the skin moisture of untreated skin.

Subsequently, the measured areas on the forearms are preconditioned as follows: They are kept under running water, approx. 32-35 ° C, for 10 seconds, then foamed with 2mg / cm ² shower bath, 10s and rinsed under running water for 15s. Subsequently, the wet areas 10s with the preparation to be tested in a

Creaming amount of 2mg / cm ² creams, washed 15s with 32-35 ° C warm water and dabbed dry with a hand towel and measured the skin moisture with the Corneometer C 825. The measurement is repeated after 1 h.

It is advantageous according to the invention if the preparation contains the acrylate copolymer in a concentration of 0.1 to 10% by weight, based on the total weight of the preparation.

It is preferred according to the invention if the preparation contains the acrylate copolymer in a concentration of 0.5 to 5% by weight, based on the total weight of the preparation.

Embodiments of the present invention which are advantageous according to the invention are characterized in that the total amount of water-soluble UV filters in the preparation is from 0.1 to 18% by weight, based on the total weight of the preparation.

It is advantageous according to the invention if sulfonic acid salts are used as water-soluble UV filters. These include 1, 4-di (2-oxo-10-sulfo-3-bomylidenemethyl) benzene and its salts; 4- (2-oxo-3-bornylidenemethyl) benzenesulfonic acid; 2-methyl-5- (2-oxo-3-bornylidenemethyl) sulfonic acid salts; Terephthalidendicamphersulfonsäure; Compounds 2-phenylbenzimidazole-5-sulfonic acid and / or salts thereof and / or phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid salts.

The counterion of the salts is usually sodium, potassium or ammonium ions, the sodium salts being preferred according to the invention.

According to the invention, the water-soluble UV filters are preferably selected from the group of the compounds 2-phenylbenzimidazole-5-sulfonic acid and / or salts thereof and / or phenylene-1,4-bis (2-benzimidazyl) -3,3'-5 , 5'-tetrasulfonsäuresalze. The use of 2-phenylbenzimidazole-5-sulfonic acid and / or salts thereof is particularly preferred according to the invention.

The preferred use concentration for 2-phenylbenzimidazole-5-sulfonic acid and / or salts thereof is from 0.1 to 8% by weight, based on the total weight of the

Preparation. According to the invention, the preparation according to the invention advantageously contains glycerol.

In such a case, advantageous embodiments of the present invention are characterized in that the preparation contains glycerol in a concentration of 0.1 to 20% by weight, based on the total weight of the preparation.

It is advantageous for the purposes of the present invention if the acrylate copolymer has a pH of 4.5 to 6.5.

The acrylate copolymer according to the invention can be purchased, for example, under the trade name Epitex 66 polymer from Dow.

It is inventively advantageous if the preparation contains one or more UV filters, which are selected from the group of compounds 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4- (1 , 1, 3,3-tetramethylbutyl) phenol); 2- (2H-Benzotriazol-2-yl) -4-methyl-6- [2-methyl-3- [1,3,3,3-tetramethyl-1 - [(trimethylsilyl) oxy] disiloxanyl] propyl] phenol ; 3- (4-methylbenzylidene) camphor; 3-benzylidenecamphor; ethylhexyl salicylate; 2-ethylhexyl-2-cyano-3,3-diphenylacrylate; 4- (dimethylamino) benzoic acid (2-ethylhexyl) ester; 4- (dimethylamino) benzoic acid amyl ester; 4-Methoxybenzalmalon-säuredi (2-ethylhexyl) ester; 4-methoxycinnamate (2-ethylhexyl) ester; Isoamyl 4-methoxycinnamate; 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone; 2,2'-dihydroxy-4-methoxybenzophenone; homomenthyl; 2-ethylhexyl 2-hydroxybenzoate;

dimethicodiethylbenzalmalonate; 3- (4- (2,2-ethoxycarbonylvinyl) phenoxy) propenyl) methoxysiloxane / dimethylsiloxane copolymer; 4- (tert-butyl) -4'-methoxydibenzoylmethane; Hexyl 2- (4'-diethylamino-2'-hydroxybenzoyl) benzoate; Dioctylbutylamidotriazone (INCI: diethylhexyl-butamidotriazone); 2,4-bis- [5-1 (dimethylpropyl) benzoxazol-2-yl- (4-phenyl) imino] -6- (2-ethylhexyl) -imino-1,3,5-triazine having the (CAS No 288254-16-0); 2,4-Bis - {[4- (2-ethylhexyloxy) -2-hydroxy] -phenyl} -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine) ; 4,4 ', 4 "- (1,3,5-triazine-2,4,6-triyltriimino) tris-benzoic acid tris (2-ethylhexyl ester) (also: 2,4,6-tris [anilino] (p-carbo-2'-ethyl-1'-hexyloxy)] - 1, 3,5-triazine (INCI: ethylhexyl triazone); 2, 4, 6-tribiphenyl-4-yl-1,3,5-triazine Merocyanines; titanium dioxide; zinc oxide.

It is preferred according to the invention if one or more compounds selected from the group 4- (tert-butyl) -4'-methoxydibenzoylmethane, ethylhexyl salicylate, homomenthyl salicylate, 2-ethylhexyl-2-cyano-3,3-diphenylacrylate as UV filter, 4,4 ', 4 "- (1,3,5-triazine-2,4,6- triyltriimino) -tris-benzoic acid tris (2-ethylhexyl ester) and 2,4-bis - {[4- (2-ethyl-hexyloxy) -2-hydroxy] -phenyl} -6- (4-methoxyphenyl) - 1, 3,5-triazine can be selected.

Embodiments which are advantageous according to the invention are furthermore characterized in that the preparation is free from propyl and butyl paraben, 3-iodo-2-propynyl butylcarbamate, methylisothiazolinone, 3- (4-methylbenzylidene) camphor and 2-hydroxy-4-methoxybenzophenone (oxybenzone ).

On the other hand, embodiments according to the invention are obtained when the preparation ethylhexylglycerol, propylene glycol, butylene glycol, 2-methylpropane-1,3-diol, 1,2-pentanediol, 1,2-hexanediol, 1,2-octanediol and / or 1,2 -Decandiol contains.

In addition, it is advantageous according to the invention if the preparation contains phenoxyethanol and / or methylparaben.

It is advantageous for the purposes of the present invention if the preparation contains one or more active substances selected from the group of the compounds magnolia extract,

Glycyrrhetinic acid, urea, arctiin, alpha-lipoic acid, folic acid, phytoene, D-biotin, coenzyme Q10, alpha-glucosylrutin, carnitine, carnosine, caffeine, natural and / or synthetic isoflavonoids, glycerylglucose, creatine, creatinine, taurine, tocopherol, tocopherol acetate, ß-alanine and / or licochalcone A contains.

It is also advantageous according to the invention if the preparation according to the invention contains one or more complexing agents. According to the invention, the use of ethylenediaminetetraacetic acid alkali metal salts (EDTA) is preferred.

According to the invention, the preparation according to the invention preferably contains from 0.02 to 1.5% by weight of EDTA, based on the total weight of the preparation.

It is also advantageous according to the invention if the preparation contains one or more

Emulsifiers selected from the group of compounds glyceryl stearate citrate,

Cetearyl Alcohol, Sodium Cetearyl Sulfate + Glyceryl Stearate, Cetearyl Sulfosuccinate

Sodium stearoyl glutamate, polyglyceryl-3-methyl glucose distearate,

Stearic acid, potassium cetyl phosphate. In this case, a content of polyglyceryl-3-methylglucose distearate is preferred according to the invention. If the preparation according to the invention contains polyglyceryl-3-methylglucose distearate, this emulsifier is used in a concentration of 0.05 to 5% by weight, based on the total weight of the preparation.

It is inventively advantageous if the preparation of the invention

Hydroxyethyl cellulose and / or acrylate / C10-30 alkyl acrylate crosspolymer contains.

Embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation contains hydroxyethylcellulose in a concentration of 0.05 to 2% by weight, based on the total weight of the preparation.

If the preparation contains acrylate / C 10-30 alkyl acrylate crosspolymer, it is

according to the invention, when this compound is used in a concentration of 0.05 to 2% by weight, based on the total weight of the preparation.

According to the invention, the preparation according to the invention may advantageously contain glycerol.

If the preparation contains glycerol, it is advantageous according to the invention if these

Compound in a concentration of 0, 1 to 20% by weight, based on the

Total weight of the preparation is used.

Embodiments which are advantageous according to the invention are also characterized in that the preparation contains ethanol.

If the preparation contains ethanol, it is preferred according to the invention if these

Compound in a concentration of 1 to 15% by weight, based on the

Total weight of the preparation is used.

The oil phase of the preparation according to the invention may also contain other oil, fat and wax components, for example, polar oils from the group of lecithins or compounds such. Cocoglyceride, caprylic / capric triglyceride, olive oil, sunflower oil, jojoba oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, castor oil, wheat germ oil, grape seed oil, thistle oil, evening primrose oil, macadamia nutol and the like. Also compounds such as phenethyl benzoate, 2-phenylethyl benzoate, isopropyl lauroyl sarcosinate, phenyl trimethicone, cyclomethicone, dibutyl adipate, octyl palmitate, octyl cocoate, octyl isostearate, octyl dodecyl myristate, octyl dodecanol, cetearyl isononanoate, Isopropyl myristate, isopropyl stearate, isopropyl oleate, n-butyl stearate, n-hexyl laurate, n-decyl oleate, isooctyl stearate, isononyl stearate, isononyl isononanoate, 2-ethylhexyl palmitate, 2-ethylhexyl laurate, 2-hexyldecyl stearate, 2-octyl dodecyl palmitate, stearyl heptanoate, oleyl oleate, oleyl erucate, Erucyl oleate, erucyl erucate, tridecyl stearate, tridecyl trimellitate can be used.

Also advantageous according to the invention are z. As natural waxes of animal and vegetable origin, such as beeswax and other insect waxes and berry wax, shea butter and / or lanolin (wool wax).

Furthermore, the oil phase can be advantageously selected from the group of dialkyl ethers and dialkyl carbonates, advantageous z. B. dicaprylyl ether (Cetiol OE) and / or Dicaprylyl- carbonate, for example, that available under the trade name Cetiol CC in the company. Cognis.

It is furthermore advantageous to use the oil component or components from the group of isoeicosane, neopentyl glycol diheptanoate, propylene glycol dicaprylate / dicaprate, caprylic / capric / diglyceryl succinate, butylene glycol dicaprylate / dicaprate, C 12-13 -alkyl lactate, di-C 12-13 -alkyl tartrate, triisostearin, dipentaerythrityl Hexacaprylate / hexacaprate, propylene glycol monoisostearate, tricaprylin, dimethylisosorbide. It is particularly advantageous if the oil phase of the formulations according to the invention has a content of Ci2-is-alkyl benzoate.

Advantageous oil components are also z. Isopropyl palmitate, myristyl myristate,

Butyl octyl salicylate (for example that available under the trade name Hallbrite BHB from the company CP Hall), tridecyl salicylate (which is available under the trade name Cosmacol ESI from the company. Sasol), C12-C15 alkyl salicylate (under the trade name Dermol NS in the company Alzo available), hexadecyl benzoate and butyl octyl benzoate and mixtures thereof (Hallstar AB).

Any mixtures of such oil and wax components are also advantageous to use in the context of the present invention.

Furthermore, the oil phase can also advantageously contain non-polar oils, for example those which are selected from the group of branched and unbranched hydrocarbons and waxes, in particular mineral oil, Vaseline (petrolatum), paraffin oil, squalane and squalene, polyolefins, hydrogenated polyisobutenes, C13- 16 isoparaffin and isohexadecane. Among the polyolefins, polydecenes are the preferred substances. It is preferred according to the invention for the preparation according to the invention to comprise dialkyl carbonate, dialkyl adipate and / or dialkyl glutarate.

According to the invention it is particularly preferred if the preparation according to the invention contains di-n-octyl carbonate (INCI dicaprylyl carbonates) and / or di-n-butyl adipate (INCI dibutyl adipate).

In addition, the preparation according to the invention may contain the customary ingredients and be composed as a conventional preparation.

The preparation of the invention can be used particularly advantageously as a daily care product or sunscreen.

It is particularly preferred according to the invention to use the preparation according to the invention as an in-shower product. Therefore, in-shower products are based on a

Inventive cosmetic preparation according to the invention.

The use of the cosmetic according to the invention is also according to the invention

Preparation as ln-shower product.

According to the invention, the use of this preparation according to the invention for the protection of the skin from UV radiation.

According to the invention, the method for protecting the skin from UV radiation, which is characterized in that a preparation according to the invention containing one or more of the present invention advantageous UV filter is applied to the wet skin after showering and then excess residues of the Preparation be rinsed by means of a water shower again.

According to the invention, drying of the skin (preferably by means of a towel) preferably follows in processes as a further process step.

Comparative test

The effect of the invention was demonstrated by way of example with the following experiment: The following formulations were prepared: 1 2 3

INCI m [%] m [%] m [%]

(Epitex 66) Acrylates Copolymer ¹ 2.0 0.0

(Comparative Polymer) Acrylates

Copolymer ² 0,0 2,0

Polyglyceryl-3 methylglucose 0.1 0.1 0.1

Distearate

Perfume 0.4 0.4 0.4

Glycerol + Aqua 1.0 1.0 1.0

Aqua + Sodium Hydroxide 0.3 0.3 0.3

Phenoxyethanol 0.5 0.5 0.5

Hydroxyethylcellulose 0.1 0.1 0.1

Acrylates / C10-30 alkyl acrylates 0.2 0.2 0.2

Crosspolymer

Carbomer 0.1 0.1 0.1

Alcohol Denat. + Aqua 10.0 10.0 10.0

Trisodium EDTA 1.0 1.0 1.0

Butyl methoxydibenzoylmethane 3,5 3,5 3,5

Phenylbenzimidazole sulfonic acid 0.1 0.1 0.1

Ethylhexyl salicylate 4,5 4,5 4,5

Ethyl hexyl triazone 1.0 1.0 1.0

Octocrylene 9.0 9.0 9.0

Homosalates 9.0 9.0 9.0

Bis-ethylhexyloxyphenol 1.0 1.0 1.0

Methoxyphenyl triazines

Diethylhexyl butamido triazone 0.5 0.5 0.5

Diethylamino hydroxybenzoyl hexyl 1.0 1.0 1.0

Benzoate

Disodium phenyl dibenzimidazole 1.0 1.0 1.0

Tetrasulfonate

Aqua ad 100 ad 100 ad 100

Amount used Epitex 66 = 4.4% by weight. This then corresponds to the specified acrylates

Crosspolymer concentration of 2% by weight (effective value)

² Daitosol 3000SLPN from Daitosakai with a glass transition temperature of + 14.5

Of these preparations, the skin moisturizing performance was as follows

Method determines:

First, in a 1. Measurement of skin hydration with the Corneometer C 825 (Courage & Khazaka) on 4 areas on the forearms. This value corresponds to the skin moisture of untreated skin. Subsequently, the measured areas on the forearms are preconditioned as follows: They are kept under running water, approx. 32-35 ° C, for 10 seconds, then foamed with 2mg / cm ² shower bath, 10s and rinsed under running water for 15s.

Subsequently, the wet areas 10s with the preparation to be tested in a

Creaming amount of 2mg / cm2 creams, wash 15s with 32-35 ° C warm water and dabbed dry with a hand towel and measured the skin moisture with the Corneometer C 825. The measurement is repeated after 1 h.

The results of the comparative experiment are shown in Figure 1.

Examples

The following examples are intended to illustrate the present invention without limiting it. Unless indicated otherwise, all amounts, proportions and percentages are based on the weight and the total amount or on the total weight of the preparations.

Crosspolymer concentration of 2% by weight (effective value)

Claims

claims

1 . Contains cosmetic preparation

a) an acrylate copolymer having a glass transition temperature of -5 to -15 C °, measured by DSC and

b) water-soluble UV filters.

2. Cosmetic preparation according to claim 1, characterized in that the

Preparation containing the acrylate copolymer in a concentration of 0.5 to 5% by weight, based on the total weight of the preparation.

3. Cosmetic preparation according to one of the preceding claims, characterized

in that sulfonic acid salts are used as water-soluble UV filters.

4. Cosmetic preparation according to one of the preceding claims, characterized

in that the water-soluble UV filters are selected from the group of the compounds 2-phenylbenzimidazole-5-sulphonic acid and / or salts thereof and / or phenylene-1,4-bis (2-benzimidazyl) -3,3'-5 , 5'-tetrasulfonsäuresalze.

5. Cosmetic preparation according to one of the preceding claims, characterized

in that the total amount of water-soluble UV filters in the preparation is from 0.5 to 18% by weight, based on the total weight of the preparation.

6. Cosmetic preparation according to one of the preceding claims, characterized

characterized in that the acrylate copolymer has a pH of 4.5 to 6.5

7. Cosmetic preparation according to one of the preceding claims, characterized

in that the preparation contains one or more UV filters which are selected from the group of the compounds 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4- (1, 1, 3,3-tetramethylbutyl) -phenol); 2- (2H-Benzotriazol-2-yl) -4-methyl-6- [2-methyl-3- [1,3,3,3-tetramethyl-1 - [(trimethylsilyl) oxy] disiloxanyl] propyl] phenol ; 3- (4-methylbenzylidene) camphor; 3-benzylidenecamphor; ethylhexyl salicylate; 2-ethylhexyl-2-cyano-3,3-diphenylacrylate; 2- (ethylhexyl) -4- (dimethylamino) benzoate; 4- (dimethylamino) benzoic acid amyl ester; Di (2-ethylhexyl) 4-methoxybenzalmalonate; 4-methoxycinnamate (2-ethylhexyl) ester; 4-methoxycinnamic acid isoamyl ester; 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone; 2,2'-dihydroxy-4-methoxybenzophenone; homomenthyl; 2-ethylhexyl 2-hydroxybenzoate; dimethicodiethylbenzalmalonate; 3- (4- (2,2-bis

Ethoxycarbonylvinyl) phenoxy) propenyl) methoxysiloxane / dimethylsiloxane copolymer; 4- (tert-butyl) -4'-methoxydibenzoylmethane; Hexyl 2- (4'-diethylamino-2'-hydroxybenzoyl) benzoate; Dioctylbutylamidotriazone (INCI: diethylhexylbutamidotriazone); 2,4-bis [5-1 (dimethylpropyl) benzoxazol-2-yl- (4-phenyl) -imino] -6- (2-ethylhexyl) -imino-1,3,5-triazine with (CAS No. 288254-16-0); 2,4-Bis - {[4- (2-ethylhexyloxy) -2-hydroxy] -phenyl} -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine) ; 4,4 ', 4 "- (1,3,5-triazine-2,4,6-triyltriimino) tris-benzoic acid tris (2-ethylhexyl ester) (also: 2,4,6-tris [anilino] (p-carbo-2'-ethyl-1'-hexyloxy)] - 1, 3,5-triazine (INCI: ethylhexyl triazone); 2,4,6-tribiphenyl-4-yl-1,3,5-triazine Merocyanines; titanium dioxide; zinc oxide.

8. Cosmetic preparation according to one of the preceding claims, characterized

in that the preparation is free from propyl and butyl paraben, 3-iodo-2-propynyl butylcarbamate, methylisothiazolinone, 3- (4-methylbenzylidene) camphor and 2-hydroxy-4-methoxybenzophenone (oxybenzone).

9. Cosmetic preparation according to one of the preceding claims, characterized

characterized in that the preparation ethylhexylglycerol, propylene glycol,

Butylene glycol, 2-methylpropane-1, 3-diol, 1, 2-pentanediol, 1, 2-hexanediol, 1, 2-octanediol and / or 1, 2-decanediol.

10. Cosmetic preparation according to one of the preceding claims, characterized

in that the preparation comprises one or more active substances selected from the group of the compounds magnolia extract, glycyrrhetinic acid, urea, arctiin, alpha-lipoic acid, folic acid, phytoene, D-biotin, coenzyme Q10, alpha-glucosylrutin, carnitine, carnosine, caffeine, natural and / or synthetic isoflavonoids,

Glyceryl glucose, creatine, creatinine, taurine, tocopherol, tocopherol acetate, β-alanine and / or licochalcone A.

1 1. Cosmetic preparation according to one of the preceding claims, characterized

in that the preparation contains phenoxyethanol and / or methylparaben.

12. Cosmetic preparation according to one of the preceding claims, characterized

in that the preparation contains one or more complexing agents.

13. Cosmetic preparation according to one of the preceding claims, characterized

in that the preparation comprises one or more emulsifiers selected from the group of the compounds glyceryl stearate citrate, cetearyl alcohol

Sodium Cetearyl Sulfate + Glyceryl Stearate, Cetearyl Sulfosuccinate

Sodium stearoyl glutamate, polyglyceryl-3-methyl glucose distearate,

Stearic acid, potassium cetyl phosphate.

14. Cosmetic preparation according to one of the preceding claims, characterized

in that the preparation contains hydroxyethyl cellulose and / or acrylate / C10-C30 alkyl acrylate crosspolymer.

15. Cosmetic preparation according to one of the preceding claims, characterized

characterized in that the preparation contains ethanol.

16. In-shower product based on a cosmetic preparation according to one of claims 1 to 15.

17. Use of a cosmetic preparation according to one of the preceding claims as an in-shower product.

18. Use of a preparation according to one of the preceding claims for protecting the skin from UV radiation.

19. A method for protecting the skin from UV radiation, characterized in that a preparation according to claim 6 to 16 after showering is applied to the wet skin and then excess residues of the preparation are rinsed by means of a water shower again.