AU698394B2 - Antiperspirant cream compositions comprising select triglyceride gellants - Google Patents
Antiperspirant cream compositions comprising select triglyceride gellantsInfo
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- AU698394B2 AU698394B2 AU76772/96A AU7677296A AU698394B2 AU 698394 B2 AU698394 B2 AU 698394B2 AU 76772/96 A AU76772/96 A AU 76772/96A AU 7677296 A AU7677296 A AU 7677296A AU 698394 B2 AU698394 B2 AU 698394B2
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Description
AJNTIPERSPIRANT CREAM COMPOSITIONS COMPRISING SELECT TRIGLYCERIDE GELLANTS
TECHNICAL FIELD
The present invention relates to antiperspirant cream compositions with improved physical stability and cosmetics. In particular, the present invention relates to antiperspirant cream compositions comprising select triglyceride gellants in combination with volatile silicone emollients.
BACKGROUND OF THE INVENTION
There are many types of topical antiperspirant products that are commercially available or otherwise known in the antiperspirant art. Most of these products are formulated as sprays, roll-on liquids, creams, or solid sticks, and comprise an astringent material, e.g. zirconium or aluminum salt, incoφorated into a suitable topical carrier. T ese products are designed to provide effective perspiration and odor control while also being cosmetically acceptable during and after application onto the axillary area or onto other areas of the skin. Aerosol sprays and solid sticks have been especially popular with consumers.
Although historically less preferred by consumers, antiperspirant creams remain an effective alternative to antiperspirant sprays and solid sticks. These creams can be applied by conventional means, or packaged into topical dispensers to make topical application more efficient and less messy. Perspiration and odor control provided by these products can be excellent. Many of these creams, however, are cosmetically unacceptable to a large number of antiperspirant users. Application of these creams can be messy, difficult to spread and wash off, and even when a cream applicator is employed, the applied areas often feel wet or sticky for several minutes after application. Many consumers have therefore preferred antiperspirant sticks for ease of administration and drier skin feel immediately after application, although the antiperspirant sticks typically leave an undesirably high residue on the skin.
One method for making more cosmetically acceptable antiperspirant creams involves dispersion of particulate antiperspirant actives in a mixture of volatile and nonvolatile solvents and silicones. These antiperspirant creams contain conventional thickening agents (e.g., bentonite clays, hectorite clays, colloidal or fumed silicas) to help maintain dispersion of the particulate antiperspirant actives over an extended period of time. The volatile silicone component provides a drier skin feel upon application to the skin, and when combined with the nonvolatile solvent provides an effective vehicle within which particulate antiperspirant actives are delivered to and deposited on the skin.
However, the conventional thickening agents used in these systems contribute a grainy texture to the product, and furthermore cannot maintain stable particulate dispersions over extended periods of time when higher volatile silicone concentrations are used. Higher volatile silicone concentrations would be desirable to further reduce stickiness, improve dry-down times after application onto skin, improve ease of spreading, and improve wash-off characteristics.
It has now been found that the antiperspirant cream compositions of the present invention, which comprise a volatile silicone solvent, particulate antiperspirant actives, and a select molar ratio of certain triglyceride gellants, provides a novel antiperspirant cream composition which delivers effective antiperspirant and odor control, and improved cosmetics (reduced stickiness, improved ease of spreading, drier-feeling application, reduced dry-down times, improved wash-off, reduced grittiness) during and after application onto skin. The triglyceride gellant material described herein, when combined with volatile silicone solvents, provides a stable structure containing a dispersion of particulate antiperspirant actives, even when higher concentrations of volatile silicones are used. These antiperspirant creams do not require the use of particulate thickening agents to establish product stability, e.g, to maintain over an extend period of time a dispersion ofthe particulate antiperspirant actives.
It is therefore an object of the present invention to provide a novel antiperspirant cream composition, and further to provide such a composition that does not necessarily require the use of particulate thickening agents, and further to provide such a composition that remains stable over extended periods even when comprised of higher concentrations of volatile silicone materials, and further to provide such a composition which provides effective antiperspirant and deodorant performance in a cosmetically acceptable cream composition.
SUMMARY OF THE INVENTION
The present invention is directed to antiperspirant compositions in a cream formulation which have a penetration force value of from about 20 gram-force to about 500 gram-force. These compositions comprise (a) from about 20% to about 80% by weight of a volatile silicone solvent; (b) from about 5% to about 35% by weight of a particulate antiperspirant active; (c) from about 0.1% to about 20% by weight of a gellant material comprising glyceryl tribehenate and other triglycerides wherein at least about 75% of the fatty acid esters moieties of said other triglycerides have from about 18 to about 36 carbon atoms, and the molar ratio of glyceryl tribehenate to said other triglycerides is from about 20:1 to about 1 :1. The present invention is also directed to a method of treating and preventing perspiration in humans by using these compositions.
DETAILED DESCRD7TION OF THE INVENTION
The antiperspirant cream compositions of the present invention are liquid dispersions of particulate solids in a continuous water-insoluble or lipophilic phase. These cream compositions are suitable for use in roll-on or topical cream applicators, or by other conventional means of topical application, for depositing antiperspirant material onto human skin.
The antiperspirant cream compositions of the present invention have a penetration force value of from about 20 gram-force to about 500 gram-force, at 27°C, 15% relative humidity, as measured with a TA-XT2 Texture Analyzer, manufactured by Texture Technology Corp, Scarsdale, New Jersey, U.S.A. This value is the force required to move a standardized 45° cone through the product, for a distance of 10 mm, at a rate of 2 mm/second. The angled cone is also available from Texture Technology Corp., as part number TA-15, and has a total cone length of about 24.7 mm, an angled cone length about 18.3 mm, a maximum diameter ofthe angled surface of the cone of about 15.5 mm. The cone is a smooth, stainless steel construction and weights about 17.8 grams. The antiperspirant cream composition of the present invention does not include solid antiperspirant stick compositions, which solid sticks have force penetration values substantially greater than about 500 gram-force, typically above about 1000 gram-force.
Preferred application of the antiperspirant compositions include roll-on application, and topical application using a cream applicator device. For roll-on application, the composition of the present invention has a penetration force value of from 20 gram-force to about 100 gram-force, preferably from about 35 gram-force to about 70 gram-force. For use as a conventional antiperspirant cream, or for use in a cream applicator device, the composition has a penetration force value of from about 100 gram- force of about 500 gram-force, preferably from about 120 gram-force to about 250 gram- force, more preferably from about 140 gram-force to about 200 gram-force.
The antiperspirant compositions of the present invention can comprise, consist of, or consist essentiaUy of the essential elements and limitations of the invention described herein, as well as any of the additional ingredients, components, or limitations described herein.
As used herein, all parts, percentages and ratios are by weight of the total composition unless otherwise specified.
Volatile Silicone Solvent
The antiperspirant composition of the present invention comprises a volatile silicone solvent at concentrations ranging from about 20% to about 80%, preferably from about 30% to about 70%, more preferably from about 45% to about 70%, by weight of
the composition. The volatile silicone of the solvent may be cyclic or linear.
"Volatile silicone" as used herein refers to those silicone materials which have measurable vapor pressure under ambient conditions. Nonlimiting examples of suitable volatile silicones are described in Todd et al., "Volatile Silicone Fluids for Cosmetics", Cosmetics and Toiletries, 91 :27-32 ( 1976), which descriptions are incoφorated herein by reference. Preferred volatile silicone materials are those having from about 3 to about 7, preferably from about 4 to about 5, silicon atoms.
Cyclic volatile silicones are preferred for use in the antiperspirant compositions herein, and include those represented by the formula:
wherein n is from about 3 to about 7, preferably from about 4 to about 5, most preferably 5. These cyclic silicone materials will generally have viscosities of less than about 10 centistokes at 25°C.
Linear volatile silicone materials suitable for use in the antiperspirant compositions include those represented by the formula:
CH, CH3 CH,
CH, — Si — Of— Si— O -Si— CH
CH3 CH, CH,
wherein n is from about 1 to about 7, preferably from about 2 to about 3. These linear silicone materials will generally have viscosities of less than about 5 centistokes at 25°C.
Specific examples of volatile silicone solvents suitable for use in the antiperspirant compositions include, but are not limited to, Cyclomethicone D-5 (commercially available from G. E. Silicones), Dow Coming 344, Dow Coming 345 and Dow Coming 200 (commercially available from Dow Coming Coφ.), GE 7207 and 7158 (commercially available from General Electric Co.) and SWS-03314 (commercially available from SWS Silicones Coφ.).
Particulate Antiperspirant Materials
The compositions of the present invention comprise particulate antiperspirant materials at concentrations ranging from about 5% to about 35%, preferably from about 10% to about 30%, antiperspirant active by weight of the compositions. These weight percentages are calculated on an anhydrous metal salt basis (exclusive of glycine, the salts of glycine, or otiier complexing agents). The particulate antiperspirant materials
preferably have particle sizes ranging from about 1 to about 100 microns, more preferably from about 1 to about 50 microns. The particulate materials may be impalpable or micro- spherical in form.
Particulate antiperspirant materials suitable for use herein are those which comprise any compound, composition or mixture thereof having antiperspirant activity. Astringent metallic salts are preferred antiperspirant materials for use herein, particularly the inorganic and organic salts of aluminum, zirconium and zinc, as well as mixtures thereof. Particularly preferred are the aluminum and zirconium salts, such as aluminum halides, aluminum hydroxy halides, zirconyl oxide halides, zirconyl hydroxy halides, and mixtures thereof.
Preferred aluminum salts are those represented by the formula:
Al2(OH)a Cl b • x H20 wherein a is from about 2 to about 5; the sum of a and b is about 6; x is from about 1 to about 6; and wherein a, b, and x may have non-integer values. Particularly preferred are the aluminum chlorhydroxides referred to as "5/6 basic chlorhydroxide", wherein a = 5, and "2/3 basic chlorhydroxide", wherein a = 4. Processes for preparing aluminum salts are disclosed in U.S. Patent 3,887,692, Gilman, issued June 3, 1975; U.S. Patent 3,904,741, Jones et al., issued September 9, 1975; U.S. Patent 4,359,456, Gosling et al., issued November 16, 1982; and British Patent Specification 2,048,229, Fitzgerald et al., published December 10, 1980, all of which are incoφorated herein by reference. Mixtures of aluminum salts are described in British Patent Specification 1,347,950, Shin et al., published February 27, 1974, also incorporated herein by reference.
Zirconium salts are also preferred for use in the antiperspirant compositions. These salts are represented by the formula:
ZrO(OH)2_aCla • x H20 wherein a is from about 1.5 to about 1.87; x is from about 1 to about 7; and wherein a and x may have non-integer values. These zirconium salts are described in Belgian Patent 825,146, Schmitz, issued August 4, 1975, incoφorated by reference herein. Particularly preferred zirconium salts are those complexes which additionally contain aluminum and glycine, commonly known as ZAG complexes. Such ZAG complexes contain aluminum chlorhydroxide and zirconyl hydroxy chloride of the formulae described above. Such ZAG complexes are described in U.S. Patent 3,679,068, Luedders et al., issued February 12, 1974; Great Britain Patent Application 2,144,992, Callaghan et al., published March 20, 1985; and U.S. Patent 4,120,948, Shelton, issued October 17, 1978, all of which are incoφorated by reference herein.
Triglyceride Gellant
The antiperspirant composition of the present invention comprises a gellant material comprising a select molar ratio of certain specified triglycerides The gellant material, when combined with the volatile silicone solvent described hereinbefore, provides the composition with a physically stable structure within which the particulate antiperspirant materials are dispersed, and maintained as such over an extended period of time.
The antiperspirant composition comprises from about 0.1% to about 20%, by weight ofthe gellant material, wherein the gellant material comprises glyceryl tribehenate and other triglycerides, wherein at least about 75%, preferably about 100%, of the esterified fatty acid moieties of said other triglycerides each have from about 18 to about 36 carbon atoms, and wherein the molar ratio of glyceryl tribehenate to said other triglycerides is from about 20: 1 to about 1 : 1, preferably from about 10: 1 to about 3: 1, more preferably from about 6:1 to about 4: 1. The esterified fatty acid moieties may be saturated or unsaturated, substituted or unsubstituted, linear or branched, but are preferably linear, saturated, unsubstituted ester moieties derived from fatty acid materials having from about 18 to about 36 carbon atoms. The triglyceride gellant material preferably has a melting point of at less than about 1 10°C, more preferably between about 60°C and 1 10°C.
It has been found that this triglyceride-based gellant material, when combined with volatile silicone solvents, and when used in the above-described molar ratio, provides a stable structure for maintaining a dispersion of particulate antiperspirant material in a topical formulation without the necessity of using conventional particulate thickening agents. This triglyceride gellant is especially useful in maintaining the physical stability of particulate dispersions containing higher concentrations of volatile silicone solvents.
It was also found that penetration force values for the antiperspirant compositions can be controlled by adjusting total triglyceride concentrations while maintaining the above-described molar ratios. In controlling penetration force values in this manner, there is no longer a need to use organic solvents or thickening agents to control penetration force values, which solvents or thickening agents often add cost to the formulation, introduce additional compatibility issues, and often contribute undesirable cosmetics such as prolonged stickiness, difficulty in ease of spreading, increased dry- down times and reduced dry feel after application.
Preferred concentrations of the gellant material ranges from about 0.5% to about 15% by weight of the composition. Specific concentrations are selected depending on the desired penetration force value. For roll-on formulations having a penetration force value of from about 20 gram-force to about 100 gram-force, triglyceride concentrations preferably range from about 1% to about 5% by weight of the antiperspirant composition.
For other cream formulations, including those formulations suitable for use in cream applicator devices, which have a penetration force value of from about 100 gram-force to about 500 gram-force, triglyceride concentrations preferably range from about 4% to about 20%, preferably from about 4% to about 10%, by weight of the antiperspirant composition.
A particularly preferred embodiment of the present invention are antiperspirant cream compositions described herein which are packaged in suitable cream applicator devices. Nonlimiting examples of suitable cream applicator devices include those described in U.S. Patent 5,000,356, which description is incoφorated herein by reference.
Specific examples of triglyceride gellants for use in the antiperspirant compositions that are commercially available include, but are not limited to, tristearin, hydrogenated vegetable oil, rape seed oil, castor wax, fish oils, tripalmiten, Syncrowax® HRC and Syncrowax® HGL-C (Syncrowax® available from Croda, Inc.).
Optional Residue Masking Material
The antiperspirant composition of the present invention may further comprise a nonvolatile emollient as a residue masking material Such materials and their use in antiperspirant products are well known in the antiperspirant art, and any such material may be incoφorated into the composition of the present invention, provided that such optional material is compatible with the essential elements of the composition, or does not unduly impair product performance or cosmetics.
Concentrations ofthe optional residue masking material ranges from about 0.1% to about 40%), preferably from about 1% to about 10%, by weight of the antiperspirant composition. These optional materials are liquid at ambient temperatures, and are non volatile. The term "non volatile" as used in this context refers to materials which have a boiling point under atmospheric pressure of at least about 200°C. Nonlimiting examples of suitable residue masking materials for use in the antiperspirant products include butyl stearate, diisopropyl adipate, petrolatum, nonvolatile silicones, octyldodecanol, phenyl trimetliicone, isopropyl myristate, C12-15 ethanol benzoate, mineral oil, and PPG- 14 Butyl Ether. Residue masking materials are described, for example, in U.S. Patent 4,985,238, which description are incoφorated herein by reference.
Optional Materials
The antiperspirant compositions of the present invention may further comprise one or more other optional materials which modify the physical characteristics of the compositions or serve as additional "active" components when deposited on the skin. Many such optional materials are known in the antiperspirant art and may be used in the
antiperspirant compositions herein, provided that such optional materials are compatible with the essential materials described herein, or do not otherwise unduly impair product performance.
Non limiting examples of optional materials include active components such as bacteriostats and fungiostats, and "non-active" components such as colorants, perfumes, cosmetic powders, emulsifiers, chelants, distributing agents, preservatives, and wash-off aids. Examples of such optional materials are described in U.S. Patent 4,049,792, Elsnau, issued September 20, 1977; Canadian Patent 1,164,347, Beckmeyer et al., issued March 27, 1984; U.S. Patent 5,019,375, Tanner et al., issued May 28, 1991; and U.S. Patent 5,429,816, Hofrichter et al., issued July 4, 1995; which descriptions are incoφorated herein by reference.
Method of Manufacture and Use
Methods for making the compositions of the present invention, as well as the equipment used in such methods, are well known to those skilled in the art. They may be batch processes involving discrete processing steps or involving continuous processes wherein the product composition is passed between processing steps in essentially continuous increments. The process may be as simple as thoroughly mixing together all of the components at the desired temperature, typically from about 35°C to about 100°C, and then allowing the heated mixture to cool to room temperature. Specific essential and non-essential materials, at specific concentrations, are selected to produce a cream of desired aesthetics and viscosity, which deposits a suitable amount of antiperspirant active on the skin during use. In making the compositions ofthe present invention care must be taken to assure mat the particulate antiperspirant materials are dispersed relatively uniformly throughout the composition.
The antiperspirant cream compositions of the present invention may be packaged in conventional antiperspirant cream containers known in the art. Such packages typically contain the cream in bulk form. The cream is then applied by hand, or by a pad or similar applicator device. These creams may also be packed in a dispenser designed to extrude or otherwise directly apply the creams to the skin. The cream compositions ofthe present invention may by packaged in known or conventional roll-on applicators, and applied to the skin by application ofthe roll-on device to the skin.
The antiperspirant compositions of the present invention are utilized in a conventional manner to treat or prevent perspiration on areas of the human body, such as the axillary areas, which are prone to perspiration wetness. Specifically, an effective amount of any ofthe compositions described herein is applied topically to such areas one or more times a day. When this is done, the compositions provide effective antiperspirant performance, as well as reduced residue on the skin, and good aesthetics upon application
for the user.
EXAMPLES
The following nonlimiting examples illustrate specific embodiments of the antiperspirant compositions of the present invention, including methods of manufacture and use.
Example I
The following describes an antiperspirant composition of the present invention. All of the listed components are combined and heated to 100°C with agitation, and cooled to 52°C. The composition is then filled into jars or cream applicators and allowed to cool and form a stiff cream. The penetration force value of the resulting composition is about 170 gram -force.
Component Weight %
Cyclomethicone D5 1 62.25
Aluminum zirconium trichlorohydrex gly 2 26.0
Butyl stearate 5.0
Glyceryl tribehenate 5.0
C18-C36 triglyceride combination- 1.25
Perfume 0.5
1 A cyclic polydimethylsiloxane containing 5 carbons, supplied by G.E. Silicones
2 Supplied by Westwood Chemical Coφoration
3 Syncrowax HGL-C, supplied by Croda, Inc.
Example H
The following describes an antiperspirant composition ofthe present invention. All of the listed components are combined and heated to 100 °C with agitation, and cooled to about 52°C. The composition is then packaged in roll-on applicators and allowed to cool. The penetration force value ofthe resulting composition is about 50 gram-force.
Component Weight %
Cyclomethicone D5 1 64.45
Aluminum zirconium trichlorohydrex gly 2 26.0
Butyl stearate 5.0
Glyceryl tribehenate 3.25
C18-C36 triglyceride combination-^ .80
Perfume 0.5
Example III
The following describes an antiperspirant composition of the present invention. The listed components are combined and heated to 100°C with agitation, and cooled to 52 °C. The composition is then packaged in jars or cream applicators and allowed to cool. The penetration force value ofthe resulting composition is about 150 gram-force
Component Weight %
Cyclomethicone D5 ' 33.75
Aluminum zirconium trichlorohydrex gly 2 26.0
Butyl stearate 33.5
Glyercyl tribehenate 5.0
C18-C36 triglyceride combination- 1.25
Perfume 0.5
Example IV
The following describes an antiperspirant composition of the present invention. The listed components are combined and heated to 100°C with agitation, and cooled to 52 °C. The composition is then packaged in jars or cream applicators and allowed to cool. The penetration force value ofthe resulting composition is about 200 gram force
Component Weight %
Cyclomethicone D5 67.25
Aluminum zirconium trichlorohydrex gly 2 26.0
Glyercyl tribehenate 5.0
C18-C36 triglyceride combination-* 1.25
Perfume 0.5
The antiperspirant compositions described in Examples I-IV, when applied to the axillary area ofthe user, provide effective prevention and control of perspiration wetness. These compositions remain physically stable over extended periods. These compositions also have reduced dry-down times, smoother and drier feel immediately after application, and reduced apparent residue.
Claims (10)
1. An antiperspirant cream composition comprising:
(a) from 20% to 80% by weight of a volatile silicone material;
(b) from 5% to 35% by weight of a particulate antiperspirant active; and
(c) from 0.1% to 20% by weight of a gellant material comprising glyceryl tribehenate and other triglycerides wherein at least 75% of the fatty acid esters moieties of said other triglycerides have from 18 to 36 carbon atoms, and the molar ratio of glyceryl tribehenate to said other triglycerides is from 20:1 to 1:1; and wherein the antiperspirant cream composition has a penetration force value of from 20 gram •force to 500 gram-force, preferably from 20 gram-force to 100 gram-force.
2. The composition of Claim 1 wherein the molar ratio is from 3:1 to 10:1, preferably from 4:1 to 6:1.
3. The composition of 2 wherein 100% of the fatty acid esters moieties of said otiier triglycerides each comprise a linear, saturated, unsubstituted carbon chain having from 18 to 36 carbon atoms.
4. The composition of Claim 2 wherein the volatile silicone material is a cyclic silicone represented by the formula
wherein n is from 3 to 7.
5. The composition of Claim 1 wherein the penetration force value is from 100 gram- force to 500 gram- force, preferably from 120 gram- force to 250 gram- force.
6. The composition of 5 wherein 100% of the fatty acid esters moieties of said other triglycerides each comprise a linear, saturated, unsubstituted carbon chain having from 18 to 36 carbon atoms.
7. The composition of Claim 5 wherein the volatile silicone material is a cyclic silicone represented by the formula wherein n is from 3 to 7.
8. The composition of any of the preceding claims, further comprising from 0.1% to 40% by weight of a residue masking material.
9. An antiperspirant cream composition comprising:
(a) from 20% to 80% by weight of a volatile cyclic silicone material;
(b) from 5% to 35% by weight of a particulate antiperspirant active;
(c) from 0.1% to 20% by weight of a gellant material comprising glyceryl tribehenate and other triglycerides wherein at least 75% ofthe fatty acid esters moieties of said other triglycerides have from 18 to 36 carbon atoms, and the molar ratio of glyceryl tribehenate to said other triglycerides is from 4: 1 to 6: 1 ; and
(d) from 0.1% to 40%, preferably from 1% to 10%, by weight of a residue masking material, preferably butyl stearate; wherein the antiperspirant cream composition has a penetration force value of from 20 gram •force to 500 gram-force.
10. A method for treating and preventing perspiration in humans comprising the topical application to tbe axillary area of an effective amount ofthe antiperspirant composition of any ofthe preceeding claims.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US55724995A | 1995-11-14 | 1995-11-14 | |
US08/557249 | 1995-11-14 | ||
US08/738,631 US5871717A (en) | 1995-11-14 | 1996-10-29 | Antiperspirant cream compositions having improved rheology |
PCT/US1996/018065 WO1997017941A1 (en) | 1995-11-14 | 1996-11-14 | Antiperspirant cream compositions comprising select triglyceride gellants |
Publications (2)
Publication Number | Publication Date |
---|---|
AU7677296A AU7677296A (en) | 1997-06-05 |
AU698394B2 true AU698394B2 (en) | 1998-10-29 |
Family
ID=27071373
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU76772/96A Ceased AU698394B2 (en) | 1995-11-14 | 1996-11-14 | Antiperspirant cream compositions comprising select triglyceride gellants |
Country Status (3)
Country | Link |
---|---|
AT (1) | ATE189383T1 (en) |
AU (1) | AU698394B2 (en) |
MX (1) | MXPA98003742A (en) |
-
1996
- 1996-11-14 AU AU76772/96A patent/AU698394B2/en not_active Ceased
- 1996-11-14 MX MXPA98003742A patent/MXPA98003742A/en active IP Right Grant
- 1996-11-14 AT AT96939649T patent/ATE189383T1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
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MXPA98003742A (en) | 2002-07-17 |
ATE189383T1 (en) | 2000-02-15 |
AU7677296A (en) | 1997-06-05 |
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