WO1998056340A1 - Perfumed compositions and methods for reducing body odors and excess moisture - Google Patents
Perfumed compositions and methods for reducing body odors and excess moisture Download PDFInfo
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- WO1998056340A1 WO1998056340A1 PCT/US1998/011811 US9811811W WO9856340A1 WO 1998056340 A1 WO1998056340 A1 WO 1998056340A1 US 9811811 W US9811811 W US 9811811W WO 9856340 A1 WO9856340 A1 WO 9856340A1
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- perfume
- cyclodextrin
- odor
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
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- 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
- A61K8/73—Polysaccharides
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- 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
- A61K8/73—Polysaccharides
- A61K8/738—Cyclodextrins
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- 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
- A61K2800/56—Compounds, absorbed onto or entrapped into a solid carrier, e.g. encapsulated perfumes, inclusion compounds, sustained release forms
Definitions
- Body odor is most commonly caused by fatty acids on skin and by malodors from microbial sources.
- the human skin is naturally populated with numerous microorganisms which are nourished by various skin secreted substances (eccrine and apocrine sweat, and sebum), skin cell debris, breakdown products of the skin and the organisms themselves.
- These unpleasant body odors are mainly organic molecules which have different structures and functional groups, such as amines, acids, alcohols, aldehydes, ketones, phenolics, polycyclics, indoles, aromatics, polyaromatics, etc. They can also be made up of sulfur-containing functional groups, such as, thiol, mercaptan, sulfide and/or disulfide groups.
- deodorant compositions aimed at combating/controlling odor associated with skin secretions, which have been described in the chemical and cosmetic literature, include emulsion sticks or suspensoid sticks, aerosols, roll-ons, pads, pump sprays, and even soap bars. These known deodorants attempt to control odor through a variety of means. For instance, U.S. Patent No. 5,525,331, to Betts, issued June 11, 1996, discloses compositions which inhibit the growth of microorganisms in the body-secretions. Deodorants may also include antibacterial compounds which help destroy/control the amount of bacteria present on skin, thereby minimizing odor produced via bacterial metabolism of skin secretions.
- Zeolites are known odor absorbers. However, these solid odor absorbers, in addition to known activated charcoal odor absorbers, lose functionality when wet. Therefore, when wetted by body fluids or when carried in an aqueous solution, these odor absorbers are not preferred as they lose their desired odor absorbent characteristics. Furthermore, zeolites can cause "harsh” feel if too much is deposited onto the skin.
- a particular advantage of the present invention is the ability to provide convenient, non-irritating odor and optionally moisture protection when applied to occluded skin areas such as the pelvic region, the external vagina, the panty-area, the bra-line, and skin-folds, which may be very sensitive.
- the aforementioned benefits may be delivered in a powder carrier which also optionally delivers skin aid benefits to the user such as protection and/or moisturization.
- the present invention relates to a perfumed powder, odor and moisture absorbing composition
- a perfumed powder, odor and moisture absorbing composition comprising from about 0.1% to about 25%, by weight of the composition, of uncomplexed cyclodextrin; optionally, from about 5% to about 60%, by weight of the composition, of a highly effective moisture absorber; a perfume composition selected from the group consisting of from about 0.05% to about 15%, by weight of the odor absorbing composition, of an encapsulated perfume, and from about 0.01% to about 5% by weight of the odor absorbing composition of a free perfume, and mixtures thereof; and a powder carrier.
- compositions of the present invention may also contain an additional odor controlling agent selected from the group consisting of zeolites, activated charcoal, sodium bicarbonate, antimicrobial agents, and antiperspirants.
- additional odor controlling agent selected from the group consisting of zeolites, activated charcoal, sodium bicarbonate, antimicrobial agents, and antiperspirants.
- the present invention also relates to methods of using the above mentioned compositions.
- the present invention relates to a perfumed dry powder composition useful in reducing body odor and moisture from occluded skin sites.
- the present invention also relates to an article of manufacture comprising the compositions herein deposited on a flexible dispensing means.
- the composition of the present invention comprises dry ingredients preferably having particle sizes of from about 1 micron to about 100 microns; more preferred from about 1 micron to about 60 microns; and most preferred from about 1 micron to about 20 microns.
- the particle size refers to the largest dimension of the particle and to the ultimate (or primary) particles.
- occluded skin refers to regions of a human or mammalian body covered by undergarments, such as the pelvic area, panty-area, and bra-line; and skin-folds or intertriginous regions, where there is continuing skin to skin contact.
- excess moisture means an undesirable and/or unhealthy level of body fluids deposited on the skin.
- body fluids includes eccrine sweat, apocrine sweat, sebum, build up of sensible moisture from transepidermal water loss, vaginal discharge, urine, and mixtures thereof.
- body odor means odors which are generated as a result of the natural functioning of a human or mammalian body. Such odors include, but are not limited to odors produced by microorganisms of the skin (i.e. bacterial decomposition of skin secretions), urine, or vaginal discharge, and mixtures thereof
- skin means human or mammalian skin.
- Entire body means the entire external surface of human or mammalian skin.
- vaginal odor relates specifically to those body odors which emanate from the pelvic region of a woman, particularly the vagina and the panty line.
- cyclodextrin includes any of the known cyclodextrins such as unsubstituted cyclodextrins containing from six to twelve glucose units, especially alpha-cyclodextrin, beta-cyclodextrin, gamma- cyclodextrin and/or their derivatives and/or mixtures thereof.
- uncomplexed cyclodextrin as used herein means that the cavities within the cyclodextrin in the composition of the present invention should remain essentially unfilled prior to application to skin in order to allow the cyclodextrin to absorb various odor molecules when the composition is applied to the skin.
- cyclodextrins for use in the present invention are alpha- cyclodextrin, beta-cyclodextrin, gamma-cyclodextrin and/or their derivatives. More preferred are beta cyclodextrin, hydroxypropyl alpha-cyclodextrin, hydroxypropyl beta-cyclodextrin, methylated-alpha-cyclodextrin or methylated-beta-cyclodextrin. Most preferred is beta-cyclodextrin.
- cyclodextrins absorb body odors more broadly by complexing with a wider range of odoriferous molecules having a wider range of molecular sizes.
- the levels of cyclodextrin are from about 0.1% to about 25%, preferably from about 1% to about 20%, more preferably from about 2% to about 15%, most preferably from about 3% to about 10%, by weight of the composition.
- Cyclodextrins having small particle sizes aid in providing higher cyclodextrin surface availability for odor absorption and therefore are preferred.
- the particle size refers to the largest dimension of the particle and to the ultimate (or primary) particles.
- Small particle cyclodextrins of this invention are those having a particle size of less than about 12 microns, preferably less than about 10 microns, and more preferably less than about 5 microns.
- Highly effective moisture absorbers are optionally included in the present invention to aid in reducing excess moisture on occluded skin and to increase the flowability (the ability to flow without caking due to moisture) of the compositions of the present invention.
- the phrase "highly effective moisture absorbers” refers to silicas (silicon dioxide), silicates or carbonates wherein the silicates and carbonates are formed by reaction of a carbonate or silicate with the alkali (IA) metals, alkaline earth (IIA) metals, or transition metals.
- Preferred highly effective moisture absorbers are calcium silicate, amorphous silicas, calcium carbonate, magnesium carbonate, or zinc carbonate, and mixtures thereof.
- Synthetic versions are formed by controlled chemical reactions in a manufacturing process rather than using a natural, mined version of these compounds which is then further refined.
- Synthetic carbonates useful in the present invention can be obtained from various suppliers such as Mallinckrodt or Whittaker, Clark, and Daniels.
- Examples of synthetic calcium silicates useful in the present invention are Hubersorb® 250 or Hubersorb® 600 available from J.M. Huber.
- the highly effective moisture absorbers comprise from about 5% to about 60%; more preferred, from about 10% to about 50%; and most preferred, from about 20% to about 40% by weight of the total composition.
- PERFUME COMPOSITION Perfume is an essential component of the present invention and is included at a level which is non-irritating to the ordinary user's skin and/or respiratory tract, yet is discernible by the human sense of smell either before and/or after application to the skin.
- the perfume compositions should be safe for use on skin.
- the perfume compositions useful herein are comprised of perfume ingredients.
- the perfume compositions can be either in the form of free perfume, in the form of encapsulated perfume, or mixtures thereof.
- the perfume composition is typically present at a level of from about 0.01% to about 20% by weight of the odor absorbing composition.
- Encapsulated Perfume It is preferred that an effective amount, typically from about 0.05% to about 15%, preferably from about 0.1% to about 10%, more preferably from about 0.2% to about 8%, and even more preferably from about 0.5% to about 5%, by weight of the odor absorbing composition, be in the form of encapsulated perfume. Encapsulating perfume helps prevent premature loss of the perfume composition to the atmosphere as well as helping avoid strong odor which can be uncomfortable to the user. As used herein, the phrase "encapsulated perfume” refers to perfume compositions which are contained in or, preferably, encapsulated in a carrier.
- encapsulation means suitable for forming the encapsulated perfume herein include formation of cyclodextrin/perfume ingredient inclusion complexes, coacervate encapsulation, cellular matrix encapsulation, crude formation of perfume-filled porous particles, and mixtures thereof.
- the encapsulated perfumes are preferably those which are released by a moisture activation mechanism whereby upon being wetted, e.g., by perspiration or other body fluids, the encapsulated perfume releases the perfume composition.
- skin irritation caused by perfume is minimized as encapsulated perfume is released only when wetted.
- Cyclodextrin/perfume ingredient inclusion complexes are preferred not only because they display the preferred moisture activation release, but also for their effectiveness and ease of processing. Perfume loading in the cyclodextrin complex is fairly low, e.g., from about 10% to about 18% in beta-cyclodextrin/perfume complex.
- the cyclodextrin/perfume ingredient inclusion complexes, particle sizes, and methods of formation useful herein, are disclosed in detail in U.S. Patent No. 5,429,628, Trinh et al., issued July 4, 1995, which is incorporated herein by reference in its entirety.
- At least an effective amount of the cyclodextrin/perfume ingredient inclusion complex is to be applied to the odor absorbing compositions herein in order to deliver the desired levels of perfume composition.
- Effective amounts are typically in the range of from about 0.01% to about 10%, preferably from about 0.1% to about 3%, more preferably from about 0.2% to about 2%, by weight of the odor absorbing composition.
- Coacervate perfume encapsulation is a commonly known encapsulation method wherein a droplet of one or more perfume ingredients is enclosed in a solid wall material.
- a solid particle contains many small droplets of one or more perfume ingredients stably held in the cells.
- Water- soluble (moisture-activated) cellular matrix perfume microcapsules which are preferred for use herein, and preparation thereof, are described in detail in U.S. Patent No. 5,429,628, Trinh et al., issued July 4, 1995, which is incorporated herein by reference in its entirety.
- Water-soluble cellular matrix perfume microcapsules useful in the present invention preferably have size of from about 0.5 micron to about 60 microns, more preferably from about 1 micron to about 50 microns, most preferably from about 2 microns to about 40 microns.
- Coacervate perfume encapsulation and cellular matrix perfume encapsulation are preferred for their perfume loading which can be as high as 60%-80%.
- Effective amounts of coacervate and/or cellular matrix perfume microcapsules are typically in the range of from about 0.002% to about 6%, preferably from about 0.007% to about 1%, more preferably from about 0.01% to about 0.5%, by weight of the odor absorbing composition.
- the crudely formed perfume-filled porous particles are used when a slow, continuous perfume composition release is desired.
- the perfume-filled porous particles are perfume ingredients/compositions which are more crudely embedded in a matrix and which release via diffusion.
- Starch matrix perfume-filled porous particles can be prepared according to the disclosure in U.S. Pat.
- porous particles starch granules
- the perfume-filled porous particles can be coated with suitable materials to improve perfume ingredient retention.
- the preferred particle size for the porous particle is from about 10 microns to about 60 microns, more preferably from about 15 microns to about 40 microns.
- the encapsulated perfume is composed of perfume ingredients selected predominantly from two groups of ingredients, namely, (a) volatile perfume ingredients having a boiling point at normal pressure of less than about 260°C, more preferably less than about 250°C, and (b) ingredients having significant low odor detection threshold, and mixtures thereof.
- the boiling points of many perfume ingredients are given in, e.g., "Perfume and Flavor Chemicals (Aroma Chemicals),” Steffen Arctander, published by the author, 1969, incorporated herein by reference in its entirety.
- at least about 50%, preferably at least about 60%, more preferably at least about 70%, and most preferably at least about 80% by weight of the encapsulated perfume is composed of perfume ingredients of the above groups (a) and (b).
- Nonlimiting examples of the more preferred volatile perfume ingredients are allo-ocimene, allyl caproate, allyl cyclohexaneacetate, allyl cyclohexanepropionate, allyl heptanoate, amyl acetate, amyl propionate, anethol, anisic aldehyde, anisole, benzaldehyde, benzyl acetate, benzyl acetone, benzyl alcohol, benzyl butyrate, benzyl formate, benzyl iso valerate, benzyl propionate, beta gamma hexenol, butyl benzoate, butyl caproate, 4-tert-butylcyclohexyl formate, camphene, camphor gum, carvacrol, laevo-carveol, d-carvone, laevo-carvone, cinnamyl formate, cis-jasmone,
- Nonlimiting examples of other preferred volatile perfume ingredients which can be used in perfume compositions of this invention are amyl benzoate, beta- caryophyllene, cinnamic alcohol, diphenyl methane, dodecalactone, ethyl methyl phenyl glycidate, eugenol, fenchyl acetate, gamma-n-methyl ionone, heliotropine, indole, isobutyl quinoline, Lilial (p-t-Bucinal), methyl-N-methyl anthranilate, para- methoxy acetophenone, phenethyl butyrate, phenyl heptanol, phenyl hexanol, and phenoxy ethyl proprionate.
- Preferred encapsulated perfume composition contain at least 5, preferably at least 6, more preferably at least 7, and even more preferably at least 8 different volatile perfume ingredients. Most common perfume ingredients which are derived from natural sources are composed of a multitude of components. When each such material is used in the formulation of encapsulated perfume compositions of the present invention, it is counted as one single ingredient, for the purpose of defining the invention.
- odor detection threshold of an odorous material means the lowest vapor concentration of that material which can be olfactorily detected.
- the odor detection threshold and some odor detection threshold values are discussed in, e.g., "Standardized Human Olfactory Thresholds", M. Devos et al, IRL Press at Oxford University Press, 1990; and "Compilation of Odor and Taste Threshold Values Data", F. A.
- Perfume ingredients that do not belong to group (a) above, but have a significantly low odor detection threshold useful herein, are selected from the group consisting of ambrox dl, bacdanol, benzyl salicylate, calone, cetalox, cis-3-hexenyl salicylate, cymal, ebanol, ethyl anthranilate, ethyl methyl phenyl glycidate, ethyl vanillin, dihydro iso jasmonate, gamma dodecalactone, flor acetate, florhydral, frutene, heliotropine, alpha ionone, beta ionone, iso eugenol, alpha isomethylionone, lilial, lyral, methyl dihydrojas
- the perfume composition may also be in the form of a free perfume.
- the term "free perfume", as used herein, means a perfume composition which is not encapsulated. Where desired, the free perfume may be diluted in a solvent to aid in incorporation into the compositions herein. Suitable solvents include the skin aids disclosed herein and solvents found in the Cosmetic Bench Reference. 1994 Edition, page 54, which is incorporated herein by reference.
- Free perfume may be composed of conventional perfume ingredients at a level of from about 0.01% to about 5%, preferably from about 0.05% to about 3%, more preferably from about 0.05% to about 2%, and most preferably from about 0.1% to about 1%, by weight of the odor absorbing composition.
- POWDER CARRIER The cyclodextrins and highly effective moisture absorbers useful in the present invention should be dispersed in a pharmaceutically-acceptable powder carrier for convenient, uniform application and disbursement onto the skin.
- pharmaceutically-acceptable means a powder suitable for topical use on the skin without undue toxicity, irritation, allergic response, and the like.
- the powder carrier also helps prevent any solubilized cyclodextrin from washing away from the desired skin contact.
- Powder carriers useful in the present invention include powders known in the art to be safe for human skin.
- Such powders include but are not limited to cornstarch (topical starch), talc, rice starch, oat starch, tapioca starch, microcrystalline cellulose (for example Avicel®), aluminum starch octenyl succinate (sold by National Starch & Chemical Co. as Dry Flo® Pure, Dry Flo® XT, and/or Dry Flo® PC), kaolin, and mixtures thereof.
- cornstarch topical starch
- talc rice starch
- oat starch tapioca starch
- microcrystalline cellulose for example Avicel®
- aluminum starch octenyl succinate sold by National Starch & Chemical Co. as Dry Flo® Pure, Dry Flo® XT, and/or Dry Flo® PC
- kaolin kaolin
- the powder carrier of the present invention will comprise from about 10% to about 95%, preferably from about 15% to about 80%, more preferably from about 25% to about 50%, by weight of the composition.
- compositions of the present invention may comprise zeolites, carbon odor-controlling agents, sodium bicarbonates, antimicrobial agents and/or antiperspirant ingredients for added body odor control.
- zeolites refers to non-fibrous zeolites. When included in the present invention, zeolites may be present from about 0.1% to about 25%, preferably from about 1% to about 15%, by weight of the composition.
- a detailed description of zeolites useful in the present invention is found in U.S. Patent No. 5,429,628, Trinh et al., issued July 4, 1995, incorporated herein by reference in its entirety.
- Carbon odor-controlling agents described in U.S. Patent No. 5,429,628 may be used in the present invention at a level of from about 0.1% to about 25%, by weight of the composition.
- Alkali metal carbonate and/or bicarbonate salts such as sodium bicarbonate, potassium bicarbonate, potassium carbonate, cesium carbonate, sodium carbonate, and mixtures thereof, may be added to the powder composition of the present invention in order to help to control acid-type odors.
- An example of sodium bicarbonate and its use as an underarm deodorant is found in U.S. Patent No. 4,382,079, to Marschner, issued May 3, 1983, which is incorporated herein in its entirety by reference.
- Preferred salts are sodium carbonate monohydrate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, and mixtures thereof.
- Alkali metal carbonate and bicarbonate salts are typically present at a level of from about 0.1% to about 30%, preferably from about 0.2% to about 20%, more preferably from about 0.3% to about 10%, by weight of the powder composition.
- the antimicrobial agents of the present invention are selected from a group consisting of antibacterial agents, antifungal agents, and mixtures thereof. Antimicrobial agents help destroy and/or control the amount of bacteria and/or fungi present on the skin.
- Preferred antimicrobial agents are zinc phenolsulfonate, zinc oxide, triclosan, Zelec® AM by DuPont, zinc ricinoleate, zinc undecylenate, and mixtures thereof. More preferred are zinc phenolsulfonate, zinc oxide, and triclosan. Triclosan is available from Ciba-Geigy as Irgasan DP-300. Examples of antimicrobial agents useful in the present invention are found in the Cosmetic Bench Reference. 1994 Edition, page 10, which is incorporated herein by reference. When included in the present invention, the antimicrobials are at a level of from about 0.01% to about 25%. Preferably from about 0.1% to about 10%, by weight of the present composition.
- antiperspirant ingredients When used on the underarms, antiperspirant ingredients may be included in the present invention. Examples of antiperspirants known in the art are found in the Cosmetic Bench Reference. 1994 Edition, page 13, which is incorporated herein by reference. When included in the present invention, antiperspirants may be present from about 0.1% to about 25%, by weight of the composition. SKTN AIDS The compositions of the present invention also optionally include skin aids.
- skin aids refers to skin protectants, emollients, and moisturizers.
- Skin protectants useful in the present invention are found in the Cosmetic Bench Reference. 1994 Edition, page 53; and the Monograph on Skin Protectant Drug Products for Over-the-Counter Human Use, 21 CFR 347.
- Preferred skin protectants are corn starch, kaolin, mineral oil, sodium bicarbonate, dimethicone, zinc oxide, colloidal oatmeal, and mixtures thereof.
- the skin protectants comprise from about 0.1% to about 80%, preferably from about 0.1% to about 30%, most preferably from about 0.1% to about 10%, by weight of the composition.
- Emollients and moisturizers useful in the present invention can be found in the Cosmetic Bench Reference. 1994 Edition, pages 27-32 and 46-48, incorporated herein by reference.
- Preferred emollients and moisturizers are tocopherol, tocopheryl acetate, aloe, vegetable oils, mineral oil, petrolatum, jojoba oil, and mixtures thereof. More preferred are encapsulated or spray/freeze dried emollients. The use of spray/freeze dried or encapsulated emollients keeps the emollients protected in the powder carrier until they are released through shearing (such as rubbing against undergarments or clothes) or through contact with skin moisture.
- the emollients/moisturizers comprise from about 0.1% to about 50%, preferably from about 0.1% to about 25%, most preferably from about 0.1% to about 10%, by weight of the composition.
- compositions may optionally comprise slip compounds.
- slip compounds refers to compounds which have unique structures which provide enhanced slip/lubrication characteristics of powders and/or reduced skin to skin friction between intertriginous skin sites.
- Slip compounds of the present invention include polyethylene; nylon; polytetra-fluoroethylene; silica which is in the form of microspheres, ellipsoids, barrel-shapes, and the like; mica, silicone (e.g. dimethicone) and metallic stearates (e.g. zinc stearate); and mixtures thereof.
- Preferred slip compounds are silicas which are in the form of microspheres, ellipsoids, barrel-shapes, and the like.
- Silica ellipsoids useful in the present invention are available from DuPont as ZELEC® Sil.
- Silica microspheres are available from KOBO as MSS-500, MSS 500/3, MSS-500/H, MSS-500/3H, MSS-500/N, and MSS-500/3N. Additionally, it is preferred that some of the silica of the present invention be fumed silica for increased flowability of the powder in addition to enhancing the slip characteristics. Fumed silica is available from Cabot Corporation (Cab-O-Sil®) and from Degussa (Aerosil®). When present in the compositions of the invention, the slip compounds comprise from about 0.1% to about 35% , preferably from about 1% to about 10%, by weight of the composition.
- the present invention may optionally also include dry or wet binders to help promote adhesion of the powder and active ingredients to the skin. Binders useful in the present invention are found in the Cosmetic Bench Reference. 1994 Edition, pages 13-14, which is incorporated herein by reference. Preferred binders are calcium stearate, zinc stearate, isopropyl myristate, magnesium myristate, silicone, and mixtures thereof. More preferred are zinc stearate, dimethicone, and mixtures thereof. When included in the composition, the binders are at a level of from about 0.1% to about 25%, preferably from about 1% to about 15%, by weight of the composition.
- Anti-pruritic agents such as those known in the art may be included in the compositions of the present invention.
- Examples of anti- pruritic agents useful in the present invention are Magnesium-L-Lactate, hydrocortisone, hydrocortisone acetate, and colloidal oatmeal. A description of anti- pruritic agents are found in the Handbook of Non Prescription Drugs. 10th Edition, p. 529, 1993; which is incorporated herein by reference.
- anti-pruritic agents may be present from about 0.1% to about 40%, by weight of the composition.
- COLORANTS Colorants and dyes can be optionally added to the odor absorbing compositions for visual appeal and performance impression. Colorants suitable for use in the present invention are found in the Cosmetic Bench Reference. 1994 Edition, pages 21-22, which is incorporated herein by reference. PROCESS OF MAKING COMPOSITIONS
- compositions of the present invention are prepared by the following steps: creating a mixture by mixing cyclodextrin, any highly effective moisture absorbers, and optional ingredients in a powder carrier via a commercially available mixer such as a vee-blender, double cone blender, or ribbon blender until the mixture is uniform; and creating a reduced size mixture using a commercially available size reduction technique such as hammer milling, impact milling, ball milling, or fluid energy milling until the desired particle size distribution is achieved.
- a commercially available mixer such as a vee-blender, double cone blender, or ribbon blender until the mixture is uniform
- a commercially available size reduction technique such as hammer milling, impact milling, ball milling, or fluid energy milling until the desired particle size distribution is achieved.
- Perfume composition may be added to the present compositions in many different ways.
- One suitable method of including encapsulated perfume involves forming cyclodextrin complexes in the manner described in U.S. Patent 5,429,628, to Trinh et al., issued July 4, 1995, which is incorporated herein by reference, and blending the perfume/cylcodextrin complexes with the composition above in a final or in an intermediate step.
- free perfume may be incorporated by spraying the cyclodextrin, carrier, or any of the powder ingredients with the free perfume.
- the free perfume is blended with one or more of the liquid ingredients herein, such as the skin aids, prior to the spraying.
- compositions of the present invention are to be applied directly to the skin or hair, various applicators are useful for delivering the compositions to the entire body for maximum odor control.
- the compositions are preferably deposited in a bottle, a canister, a spray dispenser, a manually activated spray dispenser, or on a wipe structure which later is contacted with the skin to transfer the composition to the skin.
- Bottles and canisters known in the art are suitable for use in delivering the compositions of the present invention.
- Bottles and canisters preferably comprise lids with small apertures for convenient dispensing of the composition.
- composition of the present invention can also be delivered as a suspended solution via a spray dispenser or a bottle, such that when applied or sprayed onto the skin, the solvent would immediately dry/volatilize off to leave a powder film.
- suspension forms are aerosols, liquid powder suspensions, or silicone suspensions.
- the powders of the present invention When present in an aerosol composition, the powders of the present invention will usually be present in the range of from about 0.1% to about 15%, by weight of the composition.
- the incorporation of a powder into an aerosol is more fully explained in U.S. Patent No. 4,078,051, to Pomot et al., issued March 7, 1978; which is incorporated herein by reference in its entirety. This method is not preferred however for use on sensitive areas of the body such as the panty-area or other occluded skin areas since skin irritations may result from propellants commonly used in aerosol containers.
- a manually activated spray dispenser which delivers the composition as a powder without the use of propellants, and without the composition being in a solution form.
- Spray dispensers useful herein are described more fully in U.S. Patent No. 2,450,205, to Rose, issued September 28, 1948; and U.S. Patent No. 2,840,277, to Bach, issued June 24, 1958, both of which are incorporated herein by reference in their entireties.
- the wipe comprises a flexible dispensing means.
- flexible dispensing means includes papers, cloths, non- wovens, films, foams, sponges, rollers, pads, tissues, cotton balls, and the like.
- Preferred wipe substrates comprise a porous material, such as the non-woven substrates, foams, or sponges, which are capable of holding the composition within the pores of the substrates. Examples of cellulosic non-wovens are described in U.S. Patent Number 4,191,609, Trokhan, issued March 4, 1980, which is incorporated herein by reference in its entirety.
- compositions of the present invention are well known in the art. Examples of common techniques include coating, immersing, dipping, sprinkling, or spraying, the wipe substrate with the compositions herein.
- the composition of the present invention is added to the wipe substrate at a level sufficient to provide the desired odor control and/or other desired skin benefits.
- Packages suitable for use herein are any commonly known in the art and include resealable packages and those suitable for one time use.
- the present invention also encompasses a method of reducing body odor comprising the application of an effective amount of the compositions described herein to skin.
- the present invention also encompasses a method of reducing vaginal odor comprising applying an effective amount of the compositions described herein onto a pelvic region, external vagina, and/or panty-area.
- an "effective amount" of the compositions of the present invention means an amount sufficient to absorb body odor so that it is less noticeable by the human sense of smell.
- an effective amount used and the number of uses per day is ultimately left to the discretion of the user, typically an effective amount will be from about 1 cc (cubic centimeter) to about 3 cc of odor absorbing composition per use, applied about 1 to about 3 times daily, for as many days as desired by user.
- compositions herein are topically applied directly to the skin or hair.
- the compositions can be delivered by placing the composition into a dispensing means and applying an effective amount via spraying, sprinkling, shaking, or rubbing the composition onto the desired skin surface; typically the entire body.
- the dispensing means is a sprinkling canister, a spray bottle, or a pre-formed wipe which comprises a flexible dispensing means.
- the user may deposit the composition herein onto a wipe comprising a flexible dispensing means of his or her own choosing.
- a flexible dispensing means such as a washcloth or puff; transfers the composition from a bottle or other suitable container over the chosen flexible dispensing means, and applies the composition to the desired area of the body.
- the user may also use his/her hand to apply the compositions.
- the user may use as much or as little of the composition as he/she desires, depending upon their intended use and degree of odor control necessary.
- the following non-limiting examples illustrate useful perfume compositions and odor absorbing composition formulations along with methods of use of the present invention.
- Perfume compositions A-G are all useful for formulating as encapsulated perfume.
- Perfume compositions E-G may also, optionally, be used as free perfume.
- Citronellal nitrile 1.5 Dimethyl octanol 1.6
- Linalyl acetate 8J iso Eugenol 0.3
- Citronellol 10 Benzyl salicylate 20
- Example I may also comprise an Example II may also anti-pruritic agent such as comprise a zeolite.
- Example III may also comprise a colorant.
- EXAMPLE V EXAMPLE VI -
- Example VI may also comprise sodium bicarbonate.
- Example X may also comprise Example VI may also a colorant. comprise a zeolite.
- Example VI may also comprise a zeolite.
- EXAMPLE XII EXAMPLE XIII
- Zinc Stearate 5.00 Zinc Stearate 5.00
- Tocopheryl Acetate Oil (Vit. 3.00 Mineral Oil 5.00
- Example VII may also comprise a zeolite.
- a first mixture by mixing cyclodextrin, dry ingredients, and a powder carrier in a commercially available mixer such as a vee-blender, double cone blender, or ribbon blender until the mixture is uniform; reduce the particle size of the mixture using a grinding/pulverizing technique such as hammer milling, impact milling, ball milling, or fluid energy milling; and create a second mixture by adding any liquid phase emollients, moisturizers, and/or skin protectants to the mixture, preferably using spray atomization while mixing for a more even dispersion.
- the second mixture can then undergo a second pulverizing/grinding step, and if desired, an air classifying operation.
- creating the second mixture may include the addition of the perfume compositions into the liquid phase.
- the encapsulated perfume may be added with the dry ingredients when creating the first mixture; or, preferably, may be added in a final step of creating a third mixture by adding the encapsulated perfume to the second mixture with mixing.
- the compositions of the present invention such as those formed from the examples may be loaded onto a wipe or deposited into a spray device or canister. The compositions may be applied directly onto the skin or onto a flexible dispensing means of the user's choosing for convenient application to the skin.
- Example XVII A woman with stress urinary incontinence finds that the wetness associated with this condition causes vaginal odor which she wants to remove from the skin and control. After urinating, the woman wipes her external vagina and pelvic region with a wipe containing the composition in Example X. This woman notices less vaginal odor after using the wipe.
- Example XVIII A large-breasted, obese woman finds that when she exercises, she tends to experience sweating and skin chafing under the breasts. Before and after exercising, she applies the composition from Example III or IX via a manual spray bottle. She sprays the perfumed composition under her breasts. The woman also applies the composition into intertriginous regions between her abdominal skin folds as well as other occluded skin sites. She notices less body odor and excess moisture after using the powder spray.
- Example XIX A man has severe allergies to cosmetic deodorants, antiperspirants, and heavy colognes and avoids using such products. This results in uncontrolled and embarrassing body odor. His doctor suggests applying the mild, lightly perfumed odor absorbing composition of Example I or XV after showering. The man applies the composition to his entire body via a spray each morning after showering, and suffers no allergic reaction. The man feels comfortable without the embarrassment of lingering, uncontrollable body odor. The man keeps a pouch of wipes which also contain the composition of Example I or XV, for convenient and discreet reapplication as needed.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Absorbent Articles And Supports Therefor (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU78256/98A AU7825698A (en) | 1997-06-09 | 1998-06-08 | Perfumed compositions and methods for reducing body odors and excess moisture |
JP50303099A JP2002504118A (en) | 1997-06-09 | 1998-06-08 | Aroma compositions and methods for reducing body odor and excess moisture |
HU0004370A HUP0004370A2 (en) | 1997-06-09 | 1998-06-08 | Perfumed compositions and methods for reducing body odors and excess moisture |
EP98926412A EP0988025A1 (en) | 1997-06-09 | 1998-06-08 | Perfumed compositions and methods for reducing body odors and excess moisture |
BR9810429-2A BR9810429A (en) | 1997-06-09 | 1998-06-08 | Scented compositions and methods for reproducing body odors and excess moisture |
KR19997011619A KR20010013609A (en) | 1997-06-09 | 1998-06-08 | Perfumed compositions and methods for reducing body odors and excess moisture |
CA002293663A CA2293663A1 (en) | 1997-06-09 | 1998-06-08 | Perfumed compositions and methods for reducing body odors and excess moisture |
NO996052A NO996052L (en) | 1997-06-09 | 1999-12-08 | Perfumed blends and processes to reduce body odor and excess moisture |
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87179097A | 1997-06-09 | 1997-06-09 | |
US08/871,092 | 1997-06-09 | ||
US08/871,861 US5861146A (en) | 1997-06-09 | 1997-06-09 | Method for reducing body odor |
US08/871,790 | 1997-06-09 | ||
US08/871,092 US5861143A (en) | 1997-06-09 | 1997-06-09 | Methods for reducing body odors and excess moisture |
US08/871,861 | 1997-06-09 | ||
US08/871,856 | 1997-06-09 | ||
US08/871,856 US5861144A (en) | 1997-06-09 | 1997-06-09 | Perfumed compositions for reducing body odors and excess moisture |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998056340A1 true WO1998056340A1 (en) | 1998-12-17 |
Family
ID=27505959
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1998/011811 WO1998056340A1 (en) | 1997-06-09 | 1998-06-08 | Perfumed compositions and methods for reducing body odors and excess moisture |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP0988025A1 (en) |
JP (1) | JP2002504118A (en) |
KR (1) | KR20010013609A (en) |
AU (1) | AU7825698A (en) |
BR (1) | BR9810429A (en) |
CA (1) | CA2293663A1 (en) |
CO (1) | CO4940351A1 (en) |
HU (1) | HUP0004370A2 (en) |
NO (1) | NO996052L (en) |
PE (1) | PE100099A1 (en) |
TR (1) | TR199902993T2 (en) |
WO (1) | WO1998056340A1 (en) |
Cited By (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5861147A (en) * | 1997-06-09 | 1999-01-19 | The Procter & Gamble Company | Methods for controlling environmental odors on the body using compositions comprising uncomplexed cyclodextrins and perfume |
WO2000035413A1 (en) * | 1998-12-15 | 2000-06-22 | The Procter & Gamble Company | Methods of absorbing body odors using silica containing body powders |
WO2000076472A1 (en) * | 1999-06-14 | 2000-12-21 | The Procter & Gamble Company | Anhydrous antiperspirant cream compositions having improved perfume longevity |
KR100355009B1 (en) * | 2000-12-13 | 2002-10-12 | 이계성 | cleansing agent for complexioned skin |
DE10123989A1 (en) * | 2001-05-17 | 2002-11-21 | Beiersdorf Ag | Use of salts(s) of trivalent or tetravalent metal ion with oligo- or polysaccharide(s) in composition for reducing production of and/or for removing sebum |
DE10141682A1 (en) * | 2001-08-25 | 2003-03-06 | Beiersdorf Ag | Cyclodextrin is used in production of cosmetic and dermatological compositions to give improved filler distribution on the skin |
DE10141683A1 (en) * | 2001-08-25 | 2003-03-06 | Beiersdorf Ag | Cyclodextrin is used in production of cosmetic and dermatological compositions to give improved inorganic pigment distribution on the skin |
JP2003183143A (en) * | 2001-12-18 | 2003-07-03 | Nonogawa Shoji Kk | Deodorant powdery cosmetic preparation |
WO2003089019A1 (en) * | 2002-04-18 | 2003-10-30 | The Procter & Gamble Company | Malodor-controlling compositions comprising odor control agents and microcapsules containing an active material |
EP2320879A2 (en) * | 2008-07-15 | 2011-05-18 | José. E. Fehr Pereira Lopes | Pharmaceutical composition comprising jasmonates |
US8147808B2 (en) | 2005-05-19 | 2012-04-03 | The Procter & Gamble Company | Consumer noticeable improvement in wetness protection using solid antiperspirant compositions |
US8318806B2 (en) | 2007-10-03 | 2012-11-27 | Zorbx Inc. | Deodorizing composition and method of forming thereof |
US8329154B2 (en) | 2002-04-18 | 2012-12-11 | The Procter & Gamble Company | Compositions comprising a dispersant and microcapsules containing an active material |
US8632755B2 (en) | 2005-05-19 | 2014-01-21 | The Procter & Gamble Company | Consumer noticeable improvement in wetness protection |
US8686215B2 (en) | 2009-06-18 | 2014-04-01 | The Procter amd Gamble Company | Absorbent articles comprising an odour control system |
US8883220B2 (en) | 2011-09-16 | 2014-11-11 | Nanocare Technologies, Inc. | Compositions of jasmonate compounds |
US8895041B2 (en) | 2012-03-23 | 2014-11-25 | The Procter & Gamble Company | Compositions for delivering perfume to the skin |
EP2962678A1 (en) * | 2014-06-30 | 2016-01-06 | Symrise AG | Flavour and fragrance compositions comprising acetophenone derivatives |
EP3000459A1 (en) * | 2014-09-29 | 2016-03-30 | Johnson & Johnson Consumer Inc. | Antiperspirant compositions |
WO2016072939A1 (en) * | 2014-11-07 | 2016-05-12 | National University Of Singapore | Formulations comprising antimicrobial agents with hydrophobic moieties and uses thereof |
US9439416B2 (en) | 2005-11-30 | 2016-09-13 | Eden Research Plc | Compositions and methods comprising terpenes or terpene mixtures selected from thymol, eugenol, geraniol, citral, and l-carvone |
US9480633B2 (en) | 2011-04-28 | 2016-11-01 | Kimberly-Clark Worldwide, Inc. | Temperature management composition |
US9649387B2 (en) | 2007-03-01 | 2017-05-16 | The Procter & Gamble Company | Compositions and/or articles comprising cyclodextrin complexing material |
US9655360B2 (en) | 2004-01-23 | 2017-05-23 | Eden Research Plc | Nematicidal compositions and methods of using them |
US10314918B2 (en) | 2014-12-31 | 2019-06-11 | Nanocare Technologies, Inc. | Jasmonate derivatives and compositions thereof |
US10383329B2 (en) | 2012-11-21 | 2019-08-20 | Eden Research Plc | Preservatives |
US10638750B2 (en) | 2004-05-20 | 2020-05-05 | Eden Research Plc | Compositions containing a hollow glucan particle or a cell wall particle encapsulating a terpene component, methods of making and using them |
US10667512B2 (en) | 2005-11-30 | 2020-06-02 | Eden Research Plc | Terpene-containing compositions and methods of making and using them |
US20200170901A1 (en) * | 2018-12-04 | 2020-06-04 | Henkel Ag & Co. Kgaa | Deodorant cosmetic compositions comprising calcium silicate and sodium bicarbonate |
US11000468B2 (en) | 2016-09-06 | 2021-05-11 | The Procter & Gamble Company | Aerosol compositions |
US11090250B2 (en) | 2007-03-01 | 2021-08-17 | The Procter & Gamble Company | Compositions and/or articles comprising cyclodextrin complexing material |
US11491099B2 (en) | 2016-09-06 | 2022-11-08 | The Procter & Gamble Company | Antiperspirant and deodorant compositions |
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US20080215023A1 (en) * | 2007-03-01 | 2008-09-04 | Timothy Alan Scavone | Compositions and/or articles comprising cyclodextrin complexing material |
CN102341488B (en) * | 2009-03-06 | 2013-08-14 | 株式会社资生堂 | Fragrance compositions |
KR101141797B1 (en) * | 2009-10-19 | 2012-05-04 | (주)아모레퍼시픽 | Perfume composition for expressing the fragrance of Modern Hanbang and the composition for external skin application containing the same |
JP6150984B2 (en) * | 2012-03-30 | 2017-06-21 | 大王製紙株式会社 | Scented tissue paper |
JP6019441B2 (en) * | 2012-09-28 | 2016-11-02 | 三笠製薬株式会社 | Transdermal absorption odor care tape |
WO2021149566A1 (en) * | 2020-01-20 | 2021-07-29 | 高砂香料工業株式会社 | Deodorant composition |
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US5780020A (en) * | 1996-10-28 | 1998-07-14 | The Proctor & Gamble Company | Methods and compositions for reducing body odor |
-
1998
- 1998-06-08 TR TR1999/02993T patent/TR199902993T2/en unknown
- 1998-06-08 JP JP50303099A patent/JP2002504118A/en active Pending
- 1998-06-08 CA CA002293663A patent/CA2293663A1/en not_active Abandoned
- 1998-06-08 EP EP98926412A patent/EP0988025A1/en not_active Withdrawn
- 1998-06-08 HU HU0004370A patent/HUP0004370A2/en unknown
- 1998-06-08 KR KR19997011619A patent/KR20010013609A/en not_active Application Discontinuation
- 1998-06-08 BR BR9810429-2A patent/BR9810429A/en not_active IP Right Cessation
- 1998-06-08 WO PCT/US1998/011811 patent/WO1998056340A1/en not_active Application Discontinuation
- 1998-06-08 AU AU78256/98A patent/AU7825698A/en not_active Abandoned
- 1998-06-09 CO CO98032882A patent/CO4940351A1/en unknown
- 1998-06-09 PE PE1998000483A patent/PE100099A1/en not_active Application Discontinuation
-
1999
- 1999-12-08 NO NO996052A patent/NO996052L/en not_active Application Discontinuation
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US5714445A (en) * | 1993-03-31 | 1998-02-03 | The Procter & Gamble Company | Articles containing small particle size cyclodextrin for odor control |
US5780020A (en) * | 1996-10-28 | 1998-07-14 | The Proctor & Gamble Company | Methods and compositions for reducing body odor |
Cited By (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5861147A (en) * | 1997-06-09 | 1999-01-19 | The Procter & Gamble Company | Methods for controlling environmental odors on the body using compositions comprising uncomplexed cyclodextrins and perfume |
WO2000035413A1 (en) * | 1998-12-15 | 2000-06-22 | The Procter & Gamble Company | Methods of absorbing body odors using silica containing body powders |
WO2000076472A1 (en) * | 1999-06-14 | 2000-12-21 | The Procter & Gamble Company | Anhydrous antiperspirant cream compositions having improved perfume longevity |
KR100355009B1 (en) * | 2000-12-13 | 2002-10-12 | 이계성 | cleansing agent for complexioned skin |
DE10123989A1 (en) * | 2001-05-17 | 2002-11-21 | Beiersdorf Ag | Use of salts(s) of trivalent or tetravalent metal ion with oligo- or polysaccharide(s) in composition for reducing production of and/or for removing sebum |
DE10141683A1 (en) * | 2001-08-25 | 2003-03-06 | Beiersdorf Ag | Cyclodextrin is used in production of cosmetic and dermatological compositions to give improved inorganic pigment distribution on the skin |
DE10141682A1 (en) * | 2001-08-25 | 2003-03-06 | Beiersdorf Ag | Cyclodextrin is used in production of cosmetic and dermatological compositions to give improved filler distribution on the skin |
JP2003183143A (en) * | 2001-12-18 | 2003-07-03 | Nonogawa Shoji Kk | Deodorant powdery cosmetic preparation |
WO2003089019A1 (en) * | 2002-04-18 | 2003-10-30 | The Procter & Gamble Company | Malodor-controlling compositions comprising odor control agents and microcapsules containing an active material |
US8329154B2 (en) | 2002-04-18 | 2012-12-11 | The Procter & Gamble Company | Compositions comprising a dispersant and microcapsules containing an active material |
US9655360B2 (en) | 2004-01-23 | 2017-05-23 | Eden Research Plc | Nematicidal compositions and methods of using them |
US10729130B2 (en) | 2004-01-23 | 2020-08-04 | Eden Research Plc | Nematicidal compositions and methods of using them |
US10004229B2 (en) | 2004-01-23 | 2018-06-26 | Eden Research Plc | Nematicidal compositions and methods of using them |
US10638750B2 (en) | 2004-05-20 | 2020-05-05 | Eden Research Plc | Compositions containing a hollow glucan particle or a cell wall particle encapsulating a terpene component, methods of making and using them |
US8632755B2 (en) | 2005-05-19 | 2014-01-21 | The Procter & Gamble Company | Consumer noticeable improvement in wetness protection |
US8147808B2 (en) | 2005-05-19 | 2012-04-03 | The Procter & Gamble Company | Consumer noticeable improvement in wetness protection using solid antiperspirant compositions |
US9439416B2 (en) | 2005-11-30 | 2016-09-13 | Eden Research Plc | Compositions and methods comprising terpenes or terpene mixtures selected from thymol, eugenol, geraniol, citral, and l-carvone |
US10667512B2 (en) | 2005-11-30 | 2020-06-02 | Eden Research Plc | Terpene-containing compositions and methods of making and using them |
US10258033B2 (en) | 2005-11-30 | 2019-04-16 | Eden Research Plc | Compositions and methods comprising terpenes or terpene mixtures selected from thymol, eugenol, geraniol, citral and L-carvone |
US9649387B2 (en) | 2007-03-01 | 2017-05-16 | The Procter & Gamble Company | Compositions and/or articles comprising cyclodextrin complexing material |
US11090250B2 (en) | 2007-03-01 | 2021-08-17 | The Procter & Gamble Company | Compositions and/or articles comprising cyclodextrin complexing material |
US9649386B2 (en) | 2007-03-01 | 2017-05-16 | The Procter & Gamble Company | Compositions and/or articles comprising cyclodextrin complexing material |
US8318806B2 (en) | 2007-10-03 | 2012-11-27 | Zorbx Inc. | Deodorizing composition and method of forming thereof |
EP2320879A2 (en) * | 2008-07-15 | 2011-05-18 | José. E. Fehr Pereira Lopes | Pharmaceutical composition comprising jasmonates |
EP2320879A4 (en) * | 2008-07-15 | 2014-03-05 | Pereira Lopes Jose E Fehr | Pharmaceutical composition comprising jasmonates |
US8686215B2 (en) | 2009-06-18 | 2014-04-01 | The Procter amd Gamble Company | Absorbent articles comprising an odour control system |
US9480633B2 (en) | 2011-04-28 | 2016-11-01 | Kimberly-Clark Worldwide, Inc. | Temperature management composition |
US9592305B2 (en) | 2011-09-16 | 2017-03-14 | Nanocare Technologies, Inc. | Compositions of jasmonate compounds and methods of use |
US8883220B2 (en) | 2011-09-16 | 2014-11-11 | Nanocare Technologies, Inc. | Compositions of jasmonate compounds |
US10328155B2 (en) | 2011-09-16 | 2019-06-25 | Nanocare Technologies, Inc. | Compositions of jasmonate compounds and methods of use |
US8895041B2 (en) | 2012-03-23 | 2014-11-25 | The Procter & Gamble Company | Compositions for delivering perfume to the skin |
US9364417B2 (en) | 2012-03-23 | 2016-06-14 | The Procter & Gamble Company | Compositions for delivering perfume to the skin |
US9161899B2 (en) | 2012-03-23 | 2015-10-20 | The Procter & Gamble Company | Compositions for delivering perfume to the skin |
US10383329B2 (en) | 2012-11-21 | 2019-08-20 | Eden Research Plc | Preservatives |
WO2016001263A1 (en) * | 2014-06-30 | 2016-01-07 | Symrise Ag | Flavour and fragrance compositions comprising acetophenone derivatives |
US12023396B2 (en) | 2014-06-30 | 2024-07-02 | Symrise Ag | Flavour and fragrance compositions comprising acetophenone derivatives |
EP2962678A1 (en) * | 2014-06-30 | 2016-01-06 | Symrise AG | Flavour and fragrance compositions comprising acetophenone derivatives |
RU2700412C2 (en) * | 2014-09-29 | 2019-09-17 | Джонсон энд Джонсон Консьюмер Инк. | Antiperspirant compositions |
EP3000459A1 (en) * | 2014-09-29 | 2016-03-30 | Johnson & Johnson Consumer Inc. | Antiperspirant compositions |
AU2015227433B2 (en) * | 2014-09-29 | 2021-02-04 | Johnson & Johnson Consumer Inc. | Antiperspirant compositions |
WO2016072939A1 (en) * | 2014-11-07 | 2016-05-12 | National University Of Singapore | Formulations comprising antimicrobial agents with hydrophobic moieties and uses thereof |
US10314918B2 (en) | 2014-12-31 | 2019-06-11 | Nanocare Technologies, Inc. | Jasmonate derivatives and compositions thereof |
US11000468B2 (en) | 2016-09-06 | 2021-05-11 | The Procter & Gamble Company | Aerosol compositions |
US11491099B2 (en) | 2016-09-06 | 2022-11-08 | The Procter & Gamble Company | Antiperspirant and deodorant compositions |
GB2585256A (en) * | 2018-12-04 | 2021-01-06 | Henkel Ag & Co Kgaa | Deodorant cosmetic compositions comprising calcium silicate and sodium bicarbonate |
US11090237B2 (en) | 2018-12-04 | 2021-08-17 | Henkel Ag & Co. Kgaa | Deodorant cosmetic compositions comprising calcium silicate and sodium bicarbonate |
US20200170901A1 (en) * | 2018-12-04 | 2020-06-04 | Henkel Ag & Co. Kgaa | Deodorant cosmetic compositions comprising calcium silicate and sodium bicarbonate |
GB2585256B (en) * | 2018-12-04 | 2021-09-15 | Henkel Ag & Co Kgaa | Deodorant cosmetic compositions comprising calcium silicate and sodium bicarbonate |
Also Published As
Publication number | Publication date |
---|---|
TR199902993T2 (en) | 2000-05-22 |
KR20010013609A (en) | 2001-02-26 |
HUP0004370A2 (en) | 2001-04-28 |
PE100099A1 (en) | 1999-12-02 |
NO996052L (en) | 2000-02-07 |
CO4940351A1 (en) | 2000-07-24 |
CA2293663A1 (en) | 1998-12-17 |
EP0988025A1 (en) | 2000-03-29 |
BR9810429A (en) | 2000-09-19 |
AU7825698A (en) | 1998-12-30 |
NO996052D0 (en) | 1999-12-08 |
JP2002504118A (en) | 2002-02-05 |
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