GB2050829A - Cosmetic agent comprising a pH colour indicator - Google Patents
Cosmetic agent comprising a pH colour indicator Download PDFInfo
- Publication number
- GB2050829A GB2050829A GB8015820A GB8015820A GB2050829A GB 2050829 A GB2050829 A GB 2050829A GB 8015820 A GB8015820 A GB 8015820A GB 8015820 A GB8015820 A GB 8015820A GB 2050829 A GB2050829 A GB 2050829A
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- GB
- United Kingdom
- Prior art keywords
- skin
- preparation
- red
- agent
- blue
- Prior art date
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- Granted
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0212—Face masks
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
- A61K8/355—Quinones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/45—Colour indicators, e.g. pH- or Redox indicators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/02—Preparations for care of the skin for chemically bleaching or whitening the skin
Abstract
A cosmetic agent for treating the skin comprises an acidimetric colour indicator with a transition range from pH 1.2 to 13.0 in addition to customary active cosmetic substances, moisturisers and/or cosmetic adjuvants. Preparations are applied one after the other onto the skin; the mixture of preparations is removed when the indicator changes colour.
Description
SPECIFICATION
Cosmetic agent and method for treating the skin with a cosmetic agent
This invention relates to cosmetic agents and methods of skin treatment.
As a consequence of its acidic coating the skin has its own optimal pH value of about 5 to 6. It is a known fact that successful cosmetic treatment of the skin and its structures is dependent mainly on the active hydrogen ion concentration (pH value) of the cosmetic agents being used. Use is not infrequently made of preparations which are strongly alkaline or strongly acidic, whose pH values are accordingly far removed from the optimal physiological pH value of the skin. At the conclusion of a cosmetic treatment process the skin's acidic coating should always be restored (regenerated). To effect this pH regeneration, hitherto the specifically effective preparation was generally washed off and then, if the preparation was strongly alkaline as in the case of a depilation cream, an acidic cream or tonic was applied to the skin.
In order to limit the necessary effect of strongly alkaline or strongly acidic agents on the skin to the required extent, and to restore the natural physiological conditions of the skin as soon as possible, it would be extremely useful if the course of a cosmetic treatment process could easily be observed, checked and regulated. This applies in particular for the conclusion of the course of treatment, namely regeneration of the pH in order to restore the physiological pH value of the skin.
We have also sought to provide a cosmetic agent where as large a proportion as possible of the active substances and skin-care components contained in the cosmetic agent is taken up into or deposited on the skin in a treatment time which is as short as possible and which can be exactly measured.
The invention provides a cosmetic process for treating the skin and its structures, which comprises applying a cosmetic agent that contains one or more acidimetric colour indicators and that allows the course of treatment to be regulated by means of the discernible colour change. According to the invention, the pH of the skin is regenerated following the application of strongly alkaline preparations, especially cold wave agents, depilatories or skin-softening masks, by removing the strongly alkaline preparations with cosmetic agents which contain acidimetric colour indicators with a transition range from pH 1.2 to 13.0; the treatment is concluded when the colour changes.
A similar method is employed for the pH regeneration of the skin following the application of strongly acidic preparations, especially bleaching agents for hair and skin. In this case too, according to the invention, the strongly acidic preparations are removed with cosmetic agents that have acidimetric colour indicators with a transition range from pH 1.2 to 13.0, the treatment being concluded when the colour changes.
The invention also provides an acidic or alkaline-adjusted pH regeneration agent for application to the skin and containing acidimetric colour indicators with a transition range between pH 1.2 and 13.0, in particular pH 2 to 9 and preferably pH 4 to 8.
Through the use of the cosmetic agents according to the invention a simple, visible check on the regeneration of the physiological pH value of the skin is ensured which has hitherto not been possible with the use of cosmetic agents.
The easy and safe check on the pH value during a cosmetic treatment with the help of pH indicators makes it possible to develop cosmetic agents from two or more preparations with different pH values and independent of each other as regards their use, of which at least one contains an acidimetric colour indicator.
These cosmetic agents are also subject of the invention. With their help, a guaranteed effective treatment with active substances aimed at a particular result is possible. In this way, the active substances can be controllably applied in the highly active nascent state. In addition, it is possible to obtain a hitherto unknown concentration of active substances in the skin. The "depot effect" which can thus be achieved signifies a considerable advance in cosmetic treatments.A cosmetic agent of this sort, according to the invention, consists for example of a preparation A containing the active substances and having a pH value which deviates strongly from the pH value of the skin, and a preparation B containing a pH regeneration agent for the skin; at least one of these preparations contains the acidimetric colour indicator with a transition range from pH 1.2 to 13.0, in particular pH 2 to 9 and preferably pH 4to 8. Preparation A can be strongly alkaline with a pH of about 12 to 8, especially 11 to 8, or strongly acidic with a pH of about 1.5 to 4, especially 2 to 3, according to the desired method of cosmetic treatment.
Cosmetic agents according to the invention can also consist of a strongly alkaline preparation A containing an acidimetric colour indicator, a strongly acidic preparation B and a preparation C containing a pH regeneration agent of pH about 5.0 to 6.0 for the skin and an acidimetric colour indicator with a transition rangefrom pH 1.2 to 13.0, in particularpH2to9and preferablypH4to 8. As the pH regeneration agent a buffer system is preferably used, for example, acetic acid/sodium acetate, boric acid/sodium borate, phosphoric acid/sodium phosphate or sodium bicarbonate/sodium carbonate.
The advantageous effects of such two-phase or three-phase preparations are elucidated by means of the examples. Treating the skin with an alkaline preparation A. causes swelling of the uppermost dermal layer and first makes possible, or at least considerably improves, the penetration into the skin of special active substances such as, for example, allantoin, tocopherol, lecithin, moisturising agents, collagen or uracil.
Following the necessary duration of action, the acidic preparation B is applied and mixed carefully with preparation A on the skin by massaging. The acidic preparation hardens the swollen upper dermal layer and the skin is practically sealed again once the active substances have penetrated. The process of pH regeneration, and thus the end of the treatment, has been reached when the colour indicator changes colour.
The preparations are then removed from the skin by means of damp compresses.
A two-phase treatment with a cosmetic agent where preparation A is acidic is recommendable, for example, for an optimal active substance treatment with collagen. Preparation A needs to be acidic on account of the solubility of the collagen. When regenerating the pH with preparation B the collagen precipitates and remains in intensive contact with the skin, even when the masks are removed at the end of the treatment with damp compresses.
An "active substance depot" can be obtained in the skin by means of the action of several preparations with different pH values, as can be shown using the example of a uracil-depot mask treatment. Uracil is hardly water-soluble in the acidic pH range, slightly water-soluble in the pH range of the skin and easily water-soluble in the alkaline range. This is explained by the fact that uracil is a dibasic acid with different acid constants. In order to obtain an optimal uracil depot in the skin, the treatment is carried out with three preparations which are applied one after the other. The skin is softened by the alkaline preparation A and allows the active substances to penetrate. At this pH value of e.g. 10 the uracil is easily soluble and diffuses well into the skin.For this purpose preparation A is applied generously to the parts of the skin to be treated, distributed well by massaging and left there for 2 to 8, especially 2 to 5 minutes. Following the duration of action, the preparation B, for example, an acidic face tonic with pH 2 to 3 is applied and mixed intensively, by massage, with preparation A on the skin until the colour changes. In this way the uracil is transformed into its insoluble form and remains to a large extent in the skin when the uracil mask is removed with the acidic face tonic. To complete the treatment, a pH regeneration cream (preparation C) is then applied until its colour change shows that the skin's optimal pH value of about 5.5 has been reached.
The acidimetric colour indicators suitable for purposes of the invention are in fact known. They must, however, for the purposes of the invention, be sufficiently stable in their application with respect to the active substances and other components of the cosmetic agent, reliable, and furthermore must be tolerated by the skin. The indicators which according to present-day knowledge can be considered for use in cosmetic agents are listed in the following table together with the pH range for their colour reactions and their special colour changes.
No. Indicator pH Range Colour Change
1. Tropeolin0o 1.2-3.2 violet red (Cl. 13080) yellow orange
2. Benzyl orange 1.9 - 3.3 red - yellow
3. Benzopurpurin 4B (C.I. 23560) 2.3 - 4.4 blue violet - red
4. Congo red (C.l. 22120) 3.0 - 5.2 blue - red
5. Brom-phenolblue 3.0-4.6 yellow - blue
violet
6. Bromchlorphenol blue 3.0-4.6 yellow-violet
7. Methyl orange 3.0 -4.4 red - yeliow orange (Cl. 13025) 3.5-5.7 violet pink- brownish yellow
8. a-Naphthylred 3.7-5.0 purple-yellow
orange
9. Bromcresol green 3.8-5.4 yellow - blue
10. Methyl red (Cl. 13020) 4.4-6.2 red-yellow
11. Ethyl red 4.4 - 6.2 red - yellow
12. Chlorophenol red 4.6 -7.0 yellow - red violet
13. Carminicacid (C.1.75470) 4.8 - 6.2 yellow - red violet
14. Alizarin red S (C.l. 58005) 5.0 - 6.6 yellow - violet red
No. Indicator pH Range Colour Change 15. Litmus 5.0 - 8.0 red - blue violet 16. Bromcresol purple 5.2-6.8 yellow-violet 17. Bromphenolred 5.4-7.0 yellow - purple 18. Alizarin (C.1.58000) 5.8 - 7.2 yellow - red violet 19. Bromothymol blue 6.0-7.5 yellow - blue 20. Bromxylenol blue 6.0 - 7.6 yellow - blue 21. Brasilin (C.l. 75280) 6.0 - 7.7 greenish yellow
dark violet 22.Nitrazine yellow (C.l. 14890) 6.0 - 7.0 yellow - blue violet 23. Hematoxylin (C.l. 75290) 6.0 - 11.0 yellow - violet 24. Phenol red 6.4 - 8.2 yellow - red 25. Neutral red (C.l. 50040) 6.8 - 8.0 red - yellow 26. Cresol red 0.2-1.8 pink red - yellow
7.0 - 8.8 yellow - violet red 27. m-Cresol purple 1.2-2.8 red-yellow 7.4-9.0 yellow - violet 28.Brilliant yellow
(C.l.24890) 7.4 - 8.6 yellow - brown red 29. α-Naphtholorange 7.6-8.9 yellow-pink 30. a -Naphtholphthalein 7.8 - 9.0 pale yellow - blue 31. Thymol blue 1.2-2.8 red - yellow 8.0-9.6 yellow - blue 32. Xylenolblue 1.2-2.8 red-yellow 8.0-9.6 yellow- blue 33. o-Cresolphthalein 8.2-9.8 colourless - red
violet 34. Phenolphthalein 8.4- 10.0 colourless - purple 35. a -Naphtholbenzein 8.8-11.0 colourless - blue
green 36. Thymolphthalein 9.3-10.5 colourless-blue 37. Water blue (C.1.42755) 9.4-14.0 Blue-(red)
colourless 38. Alizarin orange GG (Cl. 14025) 10.0-12.0 pale yellow- orange yellow
No.Indicator pH Range Colour Change
39. Alizarin orange R (C.l. 14030) 10.0 - 12.0 pale yellow
orange red
40. Nile blue A 10.2-13.0 blue violet red
41. (3-Naphthol violet 10.6 - 12.0 orange yellow
violet
42. Gold yellow (C.l. 14270) 11.1 - 12.7 yellow-brown red
Of the above acidimetric colour indicators, those which are differently coloured in different pH ranges are particularly useful for cosmetic treatment. These are, e.g. methyl orange, (No. 7), cresol red (No. 26), m-cresol purple, (No. 27), thymol blue, (No. 31) and xylenol blue (No. 32).
The indicators can be used in special mixtures such that pH changes can be observed by means of a continuous, manifoldly graduated colour transition.
The invention is illustrated by the following Examples.
Example 1
Face tonic for pH regeneration of the skin following application of a depilation cream.
1-Propyl alcohol 10.0 parts by weight
Perfume 0.1
Allantoin 0.2
Bromothymol blue 0.005
Eumulgin 0 10* 0.2
Phosphate buffer solution
according to Sorensen**
pH 5.5 made up to 100.0 * Emulsifying agent based on fatty alcohol or alkyl aryl polyglycol ethers ** Potassium biphosphate/disodium biphosphate solution
The preparation is yellow. A compress or wad of cotton wool is dampened with the tonic and the skin is cleaned of depilation cream. For as long as the alkaline depilation cream is not completely neutralised, the compress or wad of cotton wool is turned to blue. A colour change from yellow to blue is no longer observed when the depilation cream has been neutralised, i.e. when the physiological pH value of the skin has been reached.
Example 2
Face tonic for pH regeneration of the skin following application of a skin bleaching agent.
In order to regenerate the pH a similar face tonic is used as in Example 1, except that the tonic of Example 2 contains the indicator bromcresol green. The face tonic is thus green. For as long as the acidic face mask is not completely neutralised and the pH value of the skin regenerated, the cotton wool or compress is coloured yellow.
Example 3
pH-Regeneration emulsion for the skin following treatment with an acidic face mask.
Di-ethanolamino cetyl
phosphate (Amphisol) 3.0 parts by weight
Stearic acid 3.0 Isopropyl myristate 5.0
Paraffin oil 5.0
Phosphate buffer solution
according to Sorensen pH 5.5 9.5
Bromcresol green 0.01
Perfume 0.2
Distilled water made up to 100.0
This pH regeneration emulsion is blue and turns yellow for as long as the physiological pH value of the skin has not yet been reached. Application of the emulsion is analogous to that of the tonic according to the preceding Examples.
Example 4
Two-phase regeneration mask
Preparation A: Ointment base* 10.50 parts by weight
Squalane 6.00
Coconut oil 6.00
Distilled water 55.45
4-Hydroxybenzoic
ester 0.35
1,2-propanediol 4.00
Complex of
moisturising
factors
(Hygroplex)** 4.00
Litmus 0.20
Potassium
carbonate 0.50
Allantoin 2.00
Tocopherol
acetate 0.60
Powder mixture*** 10.00
Perfume 0.40
Preparation B: Bentonite 2.60
Glycerin 12.00
Citric acid 2.50
Distilled water 83.30
4-Hydroxybenzoic
methyl and/or
propyl ester 0.30
Sodium benzoate 0.20
Emulgin 0 10 2.00
Perfume 0.10 * Vaseline (Trade Mark), paraffin - polyethylene, triglycerides, carbohydrates, lipogel, bentonite,
cellulose derivates and/or polyethylene glycol.
** Mono- and disaccharides, amino acids, urea and weak hyperemisation substances.
Talcum, corn starch, titanium dioxide and/or wheat starch.
The pH value of preparation A is about 10. Due to its litmus content it is blue, and is applied generously onto the parts of the skin to be treated, particularly face, décolleté etc. This mask is left on the skin for about 5 minutes. The colourless, acidic preparation B (pH value 2.8) is subsequently applied to the parts of the skin to be treated and mixed carefully with preparation A on the skin by means of massage. The treatment is concluded when the acidic coating of the skin has been restored, i.e. when the blue litmus colour of the combined masks has turned to red. The preparations are then removed from the skin with damp compresses.
Example 5
Two-phase collagen mask
Preparation A: Aerosil (Trade
Mark) 3.5 parts by weight
Na-alginate 0.5
Titanium dioxide 2.0
Acidic solution
of collagen
(Collapur) 5.0
Methyl red 0.02
4-Hydroxybenzoic
methyl ester 0.18
Distilled water
made up to 100.0
Preparation B: Phosphate buffer
according to Sörensen pH 6.5
made up to 100.0
Na-caraginate
(Viscarine) 2.0
4Hydroxybenzoic 0.2
methyl ester
Preparation A is acidic and is coloured red by the indicator methyl red. It is applied generously to the parts of the skin to be treated and distributed for about 3 minutes by massaging lightly. The colourless preparation
B is subsequently applied on top of the red preparation A and the two masks mixed thoroughly on the skin until the red colour has turned completely to yellow.At the isoelectric point (pH 5 to 6) the collagen precipitates, the pH having been regenerated, and remains in contact with the skin even after the masks have been removed by treatment with damp compresses.
Example 6
Uracil-depot mask treatment
Preparation A (Alkaline uracil mask):
K-carbonate 0.2 parts by weight
Uracil 0.2
1,2-propanediol 4.0
Hydroxybenzoic
ester 0.2
Bentonite 3.0 n Bromcresol
green 0.02
Distilled water
made up to 100.0
Preparation B (Acidic face tonic):
Na-alginate 0.2 parts by weight
Citric acid 1.0
1,2-propanediol 5.0
Hydroxybenzoic
ester 0.2
Distilled water
made up to 100.0
Preparation C (pH-Regeneration uracil cream):
Emulsion according to Example 3
with 0.1 parts by weight of uracil.
The blue preparation A, which contains the dissolved uracil, is applied generously to the parts of the skin to be treated, distributed well by massaging and left on for a further 3 to 5 minutes. After the duration of action the colourless, acidic face tonic (preparation B) with pH value 2.8 is applied and mixed intensively with mask A by massaging until the blue colour has turned completely to yellow. This causes the uracil to precipitate. Finally a pH regeneration cream C which contains uracil is applied, the uracil content of which increases the uracil depot which has already been worked into the skin and which is only slightly soluble in the pH range of the skin. The blue cream C, applied with a ball of cotton wool, is coloured yellow for as long as the optimal skin pH value of about 5.5 has not been reached.The preparation C may contain a further indicator, e.g. bromothymol blue, or may be used without an indicator.
Example 7
Two-phase regeneration mask
Preparation A: Amorphous
silicic acid
(Aerosil) 9.000 parts by weight
Corn starch 2.000
Allantoin 2.000 11 1,2 Dipropyl
alcohol 6.000
Panthenol 1.200
4-Hydroxy
benzoic methyl
ester 0.0002
4-Hydroxy
benzoic propyl
ester 0.00006
Alizarin 0.00002
Triethanolamine 2.000
Extract of
wheatgerm
(Epigran) 4.000
Emulgin 010 0.0001
Tocopherol
acetate 0.0006
Distilled H2O made up to 100.000
Preparation B: (Teginacid)* 5.000
(Emulgade F
Spezial)** 4.000
Isopropyl
myristate 5.000 Cetyl stearyl alcohol mixture 1.000
Mixture of
triglycerides
(Miglyol 812) 5.000
1,2-propane
diol 4.000
Moisturising
agent
(Hygroplex)*** 4.000
4-Hydroxy
benzoic methyl
ester 0.0002
4-Hydroxy
benzoic propyl
ester 0.0001
Na-benzoate 0.0002
Lactic acid 2.000
Distilled H2O made up to 100.000 * o/w emulsifying agent of glycerin mono-distearates and polyglycol fatty alcohol ether ** Emulsifying agent based on cetyl stearyl alcohol with addition of cetyl stearyl sulphate - Na or
non-ionic polyglycol ether Mono- and disaccharides, amino acids, urea and weak hyperemisation substances.
The pH value of preparation A, which is blue-violet in colour, is about 8.2. It is applied to the skin, where it is allowed to take effect for about 5 minutes. During this time the skin swells, which results in better or increased uptake of the active substances. Then the colourless, acidic preparation B with pH 2.6 is applied and mixed with the preparation A already on the skin until the colour turns to yellow. The mixture of preparations is then removed from the skin.
Claims (16)
1. Tropeolin00 (C.l. 13080)
2. Benzyl orange
3. Benzopurpurin 4B (C.l. 23560)
4. Congo red (C.l. 22120)
5. Brom-phenol blue
6. Bromchlorphenol blue
7. Methyl orange (C.l. 13025)
8. a-Naphthyl red
9. Bromcresol green
10. Methyl red (C.l. 13020)
11. Ethyl red
12. Chlorophenol red
13. Carminicacid (C.l. 75470)
14. Alizarin red S (C.l. 58005)
15. Litmus
16. A method of treating the skin with a cosmetic agent, substantially as hereinbefore described with reference to any of the Examples.
16. Bromcresol purple
17. Bromphenol red
18. Alizarin (C.l. 58000) 19.Bromothymol blue
20. Bromxylenol blue
21. Brasilin (C.l. 75280)
22. Nitrazineyellow (C.1.14890)
23. Hematoxylin (C.l. 75290)
24. Phenol red
25. Neutral red (C.l. 50040)
26. Cresol red
27. m-Cresol purple
28. Brilliant yellow (C.l. 24890)
29. a-Naphtholorange
30. a-Naphtholphthalein
31. Thymol blue
32. Xylenol blue
33. o-Cresolphthalein
34. Phenolphthalein
35. a-Naphtholbenzein
36. Thymolphthalein
37. Water blue (C.l. 42755)
38. Alizarin orange GG (C.l. 14025)
39. Alizarin orange R (C.l. 14030)
40. Nile blue A
41. p-Naphthol violet 42. Gold yellow (C.l. 14270)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19792919422 DE2919422C3 (en) | 1979-05-15 | 1979-05-15 | Cosmetic agent and process for its manufacture |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2050829A true GB2050829A (en) | 1981-01-14 |
GB2050829B GB2050829B (en) | 1983-10-26 |
Family
ID=6070710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8015820A Expired GB2050829B (en) | 1979-05-15 | 1980-05-13 | Cosmetic agent comprising a ph colour indicator |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE2919422C3 (en) |
FR (1) | FR2456518A1 (en) |
GB (1) | GB2050829B (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU633952B2 (en) * | 1990-02-07 | 1993-02-11 | Nasser Norman Tehrani | Rapid hair ph indication and solution therefor |
WO1994026233A1 (en) * | 1993-05-13 | 1994-11-24 | Fuerst Ronnie S | Novel materials and methods utilizing a temporary visual indicator |
EP0820761A2 (en) * | 1996-07-27 | 1998-01-28 | Coreana Cosmetics Co., Ltd. | Tanning cosmetics containing caesapinia sappan L. extract |
US5837645A (en) * | 1993-05-13 | 1998-11-17 | Fuerst; Ronnie S. | Materials and methods utilizing a temporary visual indicator |
FR2902322A1 (en) * | 2006-06-15 | 2007-12-21 | A2P Sas Soc Par Actions Simpli | Acid-based exfoliating composition useful for cosmetic treatment of the skin comprises a colored pH indicator |
WO2008060355A2 (en) * | 2006-10-03 | 2008-05-22 | Allegiance Corporation | Color change surgical prep solution |
US7858568B2 (en) | 2003-08-29 | 2010-12-28 | Kimberly-Clark Worldwide, Inc. | Single phase color change agents |
CN103030533A (en) * | 2011-09-29 | 2013-04-10 | 苏州百灵威超精细材料有限公司 | Process for synthesizing bis(4-hydroxy-1-naphthyl)benzyl alcohol |
US11273112B2 (en) | 2017-12-21 | 2022-03-15 | L'oreal | Process for treating keratin fibers using a halochromic triarylmethane direct dye, an alkaline revealer and then an acidic eraser |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0471105B1 (en) * | 1990-08-16 | 1996-11-06 | Norman Tehrani Nasser | Rapid hair pH indication and solution therefor |
US8067350B2 (en) | 2005-12-15 | 2011-11-29 | Kimberly-Clark Worldwide, Inc. | Color changing cleansing composition |
CN110785161B (en) | 2017-06-23 | 2023-06-20 | 宝洁公司 | Compositions and methods for improving the appearance of skin |
KR20210011964A (en) | 2018-07-03 | 2021-02-02 | 더 프록터 앤드 갬블 캄파니 | How to treat a skin condition |
JP2023528616A (en) | 2020-06-01 | 2023-07-05 | ザ プロクター アンド ギャンブル カンパニー | Method for improving skin penetration of vitamin B3 compounds |
US10959933B1 (en) | 2020-06-01 | 2021-03-30 | The Procter & Gamble Company | Low pH skin care composition and methods of using the same |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB498890A (en) * | 1937-07-15 | 1939-01-16 | Robert Edwin Goldsbrough | Improvements in and relating to the manufacture of creams and lotions for toilet purposes |
US2496270A (en) * | 1946-02-09 | 1950-02-07 | Synergistics Inc | Skin dressings with fugitive colors |
DE1492164C3 (en) * | 1964-03-21 | 1975-09-25 | Hans Schwarzkopf Gmbh, 2000 Hamburg | Wave agent aerosol preparation |
FR1499925A (en) * | 1966-04-05 | 1967-11-03 | Marie Jeanne Niederhof | Process for the preparation of a bubble bath intended for the maintenance of the skin and for combating the peripheral manifestations of fatigue, while slowing the effects of aging on the integuments |
FR2021291A5 (en) * | 1969-09-11 | 1970-07-17 | Clavel Louis | Foaming bath colourant |
GB1313180A (en) * | 1970-09-23 | 1973-04-11 | Unilever Ltd | Surface active liquids |
JPS5016364B1 (en) * | 1970-11-25 | 1975-06-12 |
-
1979
- 1979-05-15 DE DE19792919422 patent/DE2919422C3/en not_active Expired
-
1980
- 1980-05-13 GB GB8015820A patent/GB2050829B/en not_active Expired
- 1980-05-14 FR FR8010923A patent/FR2456518A1/en active Pending
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU633952B2 (en) * | 1990-02-07 | 1993-02-11 | Nasser Norman Tehrani | Rapid hair ph indication and solution therefor |
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US5523075A (en) * | 1993-05-13 | 1996-06-04 | Fuerst; Ronnie S. | Materials and methods utilizing a temporary visual indicator |
US5837645A (en) * | 1993-05-13 | 1998-11-17 | Fuerst; Ronnie S. | Materials and methods utilizing a temporary visual indicator |
US5997891A (en) * | 1993-05-13 | 1999-12-07 | Ipa, Llc | Materials and methods utilizing a temporary visual indicator |
US6139821A (en) * | 1993-05-13 | 2000-10-31 | Ipa, Llc | Materials and methods utilizing a temporary visual indicator |
EP0820761A2 (en) * | 1996-07-27 | 1998-01-28 | Coreana Cosmetics Co., Ltd. | Tanning cosmetics containing caesapinia sappan L. extract |
EP0820761A3 (en) * | 1996-07-27 | 1998-07-29 | Coreana Cosmetics Co., Ltd. | Tanning cosmetics containing caesapinia sappan L. extract |
US7858568B2 (en) | 2003-08-29 | 2010-12-28 | Kimberly-Clark Worldwide, Inc. | Single phase color change agents |
FR2902322A1 (en) * | 2006-06-15 | 2007-12-21 | A2P Sas Soc Par Actions Simpli | Acid-based exfoliating composition useful for cosmetic treatment of the skin comprises a colored pH indicator |
WO2008060355A3 (en) * | 2006-10-03 | 2009-07-09 | Allegiance Corp | Color change surgical prep solution |
WO2008060355A2 (en) * | 2006-10-03 | 2008-05-22 | Allegiance Corporation | Color change surgical prep solution |
US9101134B2 (en) | 2006-10-03 | 2015-08-11 | Carefusion 2200, Inc. | Color change surgical prep solution |
CN103030533A (en) * | 2011-09-29 | 2013-04-10 | 苏州百灵威超精细材料有限公司 | Process for synthesizing bis(4-hydroxy-1-naphthyl)benzyl alcohol |
CN103030533B (en) * | 2011-09-29 | 2014-12-10 | 苏州百灵威超精细材料有限公司 | Process for synthesizing bis(4-hydroxy-1-naphthyl)benzyl alcohol |
US11273112B2 (en) | 2017-12-21 | 2022-03-15 | L'oreal | Process for treating keratin fibers using a halochromic triarylmethane direct dye, an alkaline revealer and then an acidic eraser |
Also Published As
Publication number | Publication date |
---|---|
DE2919422A1 (en) | 1980-11-20 |
FR2456518A1 (en) | 1980-12-12 |
DE2919422C3 (en) | 1982-05-19 |
DE2919422B2 (en) | 1981-07-09 |
GB2050829B (en) | 1983-10-26 |
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