JP2004502709A5 - - Google Patents
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- Publication number
- JP2004502709A5 JP2004502709A5 JP2002508383A JP2002508383A JP2004502709A5 JP 2004502709 A5 JP2004502709 A5 JP 2004502709A5 JP 2002508383 A JP2002508383 A JP 2002508383A JP 2002508383 A JP2002508383 A JP 2002508383A JP 2004502709 A5 JP2004502709 A5 JP 2004502709A5
- Authority
- JP
- Japan
- Prior art keywords
- propellant
- agents
- aerosol
- composition
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 description 26
- 239000000443 aerosol Substances 0.000 description 20
- 239000003795 chemical substances by application Substances 0.000 description 19
- 239000003380 propellant Substances 0.000 description 19
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 10
- 239000007921 spray Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 7
- 230000000507 anthelmentic effect Effects 0.000 description 7
- -1 2-ethylhexyl group Chemical group 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000002781 deodorant agent Substances 0.000 description 6
- 239000000921 anthelmintic agent Substances 0.000 description 5
- 229940124339 anthelmintic agent Drugs 0.000 description 5
- 239000002537 cosmetic Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 241000021559 Dicerandra Species 0.000 description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 4
- 235000010654 Melissa officinalis Nutrition 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000006750 UV protection Effects 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000865 liniment Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 230000008961 swelling Effects 0.000 description 4
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 4
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 3
- 230000001166 anti-perspirative effect Effects 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 239000003213 antiperspirant Substances 0.000 description 3
- 230000000035 biogenic effect Effects 0.000 description 3
- 239000007854 depigmenting agent Substances 0.000 description 3
- OKQDSOXFNBWWJL-UHFFFAOYSA-N dihexyl carbonate Chemical compound CCCCCCOC(=O)OCCCCCC OKQDSOXFNBWWJL-UHFFFAOYSA-N 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000003752 hydrotrope Substances 0.000 description 3
- 239000000787 lecithin Substances 0.000 description 3
- 229940067606 lecithin Drugs 0.000 description 3
- 235000010445 lecithin Nutrition 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 150000003904 phospholipids Chemical class 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 239000003124 biologic agent Substances 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical group OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 2
- PKPOVTYZGGYDIJ-UHFFFAOYSA-N dioctyl carbonate Chemical compound CCCCCCCCOC(=O)OCCCCCCCC PKPOVTYZGGYDIJ-UHFFFAOYSA-N 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- BJRNKVDFDLYUGJ-RMPHRYRLSA-N hydroquinone O-beta-D-glucopyranoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-RMPHRYRLSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 150000003077 polyols Chemical group 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 0 CC1C(C)*(C)CC1 Chemical compound CC1C(C)*(C)CC1 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 208000001840 Dandruff Diseases 0.000 description 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 1
- VZRKEAFHFMSHCD-UHFFFAOYSA-N Ethyl 3-(N-butylacetamido)propionate Chemical compound CCCCN(C(C)=O)CCC(=O)OCC VZRKEAFHFMSHCD-UHFFFAOYSA-N 0.000 description 1
- MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000004904 UV filter Substances 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229960000271 arbutin Drugs 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229940086555 cyclomethicone Drugs 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 229940120503 dihydroxyacetone Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001093 holography Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- BEJNERDRQOWKJM-UHFFFAOYSA-N kojic acid Chemical compound OCC1=CC(=O)C(O)=CO1 BEJNERDRQOWKJM-UHFFFAOYSA-N 0.000 description 1
- 229960004705 kojic acid Drugs 0.000 description 1
- WZNJWVWKTVETCG-UHFFFAOYSA-N kojic acid Natural products OC(=O)C(N)CN1C=CC(=O)C(O)=C1 WZNJWVWKTVETCG-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- BJRNKVDFDLYUGJ-UHFFFAOYSA-N p-hydroxyphenyl beta-D-alloside Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10033022.3 | 2000-07-07 | ||
| DE10033022A DE10033022A1 (de) | 2000-07-07 | 2000-07-07 | Aerosole |
| PCT/EP2001/007514 WO2002003927A2 (de) | 2000-07-07 | 2001-06-30 | Desodorierende zubereitungen mit einem gehalt an dialkylcarbonaten und treibmitteln und deren verwendung als aerosole |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004502709A JP2004502709A (ja) | 2004-01-29 |
| JP2004502709A5 true JP2004502709A5 (enExample) | 2008-08-21 |
| JP4909485B2 JP4909485B2 (ja) | 2012-04-04 |
Family
ID=7648108
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002508383A Expired - Lifetime JP4909485B2 (ja) | 2000-07-07 | 2001-06-30 | エアゾール |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7427406B2 (enExample) |
| EP (1) | EP1299074B1 (enExample) |
| JP (1) | JP4909485B2 (enExample) |
| KR (1) | KR20030040349A (enExample) |
| CN (1) | CN1440271A (enExample) |
| AU (1) | AU2001295170A1 (enExample) |
| DE (2) | DE10033022A1 (enExample) |
| ES (1) | ES2259039T3 (enExample) |
| WO (1) | WO2002003927A2 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10162049A1 (de) * | 2001-12-17 | 2003-06-26 | Cognis Deutschland Gmbh | Antitranspirant-Zusammensetzung |
| ES2410587T3 (es) | 2004-01-22 | 2013-07-02 | University Of Miami | Formulaciones tópicas de coenzima Q10 y métodos de uso |
| US20050249686A1 (en) * | 2004-04-27 | 2005-11-10 | Francoise Pataut | Cosmetic composition free of water comprising fatty acid esters, petrolatum oil and non-ionic polymers |
| EP1602351A1 (en) * | 2004-05-24 | 2005-12-07 | The Procter & Gamble Company | High coverage cosmetic foundation |
| DE102005001820A1 (de) | 2005-01-13 | 2006-08-10 | Beiersdorf Ag | Haarsprayformeln mit hohen VOC-Anteilen und mit einem Terpolymer aus Methacrylsäure, Methylmethacrylat, Hydroxyethylmethacrylat und Butylacrylat |
| DE102005060788A1 (de) * | 2005-12-16 | 2007-06-28 | Beiersdorf Ag | Verbesserte Langzeitwirkung von Antitranspirantien |
| GB0601644D0 (en) * | 2006-01-27 | 2006-03-08 | Unilever Plc | Antiperspirant compositions |
| EP1932504A1 (en) * | 2006-11-07 | 2008-06-18 | KPSS-Kao Professional Salon Services GmbH | Composition for keratin fibres |
| EP1920753A1 (en) * | 2006-11-07 | 2008-05-14 | KPSS-Kao Professional Salon Services GmbH | Composition for keratin fibres |
| MX337408B (es) | 2007-03-22 | 2016-03-03 | Berg Llc | Formulaciones topicas que tienen biodisponibilidad aumentada. |
| WO2009126764A1 (en) | 2008-04-11 | 2009-10-15 | Cytotech Labs, Llc | Methods and use of inducing apoptosis in cancer cells |
| EA023913B1 (ru) * | 2009-05-11 | 2016-07-29 | БЕРГ ФАРМА ЭлЭлСи | Способы лечения метаболических нарушений, использующие эпиметаболические переключатели, многоаспектные внутриклеточные молекулы или факторы влияния |
| MX341433B (es) * | 2009-12-23 | 2016-08-18 | Colgate-Palmolive Company * | Composicion antitranspirante/desodorante anhidra liquida. |
| KR101907411B1 (ko) | 2010-03-12 | 2018-10-12 | 베르그 엘엘씨 | 코엔자임 Ｑ10(ＣｏＱ10)의 정맥내 제형 및 이의 사용 방법 |
| DE102010050774A1 (de) | 2010-11-10 | 2012-05-10 | Beiersdorf Ag | Kosmetisches Sonnenschutzspray |
| CN103608323B (zh) | 2011-04-04 | 2016-08-17 | 博格有限责任公司 | 治疗中枢神经系统肿瘤的方法 |
| CN107095863A (zh) | 2011-06-17 | 2017-08-29 | 博格有限责任公司 | 可吸入药物组合物 |
| CN109223589A (zh) * | 2011-11-23 | 2019-01-18 | 巴斯夫欧洲公司 | 油凝胶在uv吸收剂组合物中的用途 |
| EP2983654B1 (en) | 2013-04-08 | 2025-11-12 | BPGbio, Inc. | Treatment of cancer using coenzyme q10 combination therapies |
| WO2015035094A1 (en) | 2013-09-04 | 2015-03-12 | Berg Llc | Methods of treatment of cancer by continuous infusion of coenzyme q10 |
| JP5907213B2 (ja) * | 2014-05-28 | 2016-04-26 | 株式会社ヒロマイト | 炭酸ガスを溶解した油組成物及びその用途 |
| JP5907214B2 (ja) * | 2014-06-16 | 2016-04-26 | 株式会社ヒロマイト | 炭酸ガスを溶解したエマルジョン組成物及びその用途 |
| GB2534355B (en) * | 2015-01-09 | 2017-04-05 | Ryan Sy Von | A composition, method, apparatus for a sprayable cleaning product |
| CN104988797A (zh) * | 2015-05-28 | 2015-10-21 | 句容市茂源织造厂 | 一种铜版纸防霉除臭剂 |
| US20170189350A1 (en) | 2015-11-16 | 2017-07-06 | Berg Llc | Methods of treatment of temozolomide-resistant glioma using coenzyme q10 |
| WO2019069209A1 (en) | 2017-10-02 | 2019-04-11 | Tbf Environmental Technology Inc. | SOLVENT COMPOUNDS FOR USE AS AGENTS OF COALESCENCE |
| KR20180102035A (ko) | 2018-09-05 | 2018-09-14 | (주)아모레퍼시픽 | 디카프릴릴 카보네이트를 함유하는 입술용 화장료 조성물 |
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| DE1165574B (de) | 1960-08-08 | 1964-03-19 | Dehydag Gmbh | Verfahren zur Herstellung von als Emulgiermittel fuer Salbengrundlagen dienenden Mischestern |
| DE2024051C3 (de) | 1970-05-16 | 1986-05-07 | Henkel KGaA, 4000 Düsseldorf | Verwendung der Veresterungsprodukte von Glycerin-Äthylenoxid-Addukten mit Fettsäuren als Rückfettungsmittel in kosmetischen Zubereitungen |
| DE2366186A1 (enExample) * | 1973-05-26 | 1978-08-24 | ||
| US4172887A (en) | 1973-11-30 | 1979-10-30 | L'oreal | Hair conditioning compositions containing crosslinked polyaminopolyamides |
| LU68901A1 (enExample) | 1973-11-30 | 1975-08-20 | ||
| JPS55142073A (en) * | 1979-04-23 | 1980-11-06 | Toyo Aerosol Kogyo Kk | Aerosol composition |
| US5098886A (en) * | 1991-03-17 | 1992-03-24 | Narula Anubhav P S | Substituted and unsubstituted alkyl cyclohexylmenthyl and cyclohexenylmethyl carbonates and perfumery uses thereof |
| DE4119890A1 (de) | 1991-06-17 | 1992-12-24 | Henkel Kgaa | Kosmetische und pharmazeutische oelkomponente |
| GB9214765D0 (en) | 1992-07-11 | 1992-08-26 | Smithkline Beecham Plc | Pressurised aerosol formulation |
| WO1995016824A1 (en) | 1993-12-13 | 1995-06-22 | The Procter & Gamble Company | Lotion composition for imparting soft, lubricious feel to tissue paper |
| US5830487A (en) | 1996-06-05 | 1998-11-03 | The Procter & Gamble Company | Anti-viral, anhydrous, and mild skin lotions for application to tissue paper products |
| JP3159420B2 (ja) * | 1994-04-14 | 2001-04-23 | カネボウ株式会社 | 油性化粧料 |
| CA2192177A1 (en) | 1994-06-17 | 1995-12-28 | Thomas James Klofta | Improved lotion composition for treating tissue paper |
| CN1106481C (zh) | 1994-06-17 | 2003-04-23 | 普罗克特和甘保尔公司 | 洗剂处理过的薄页纸 |
| DE4426215A1 (de) | 1994-07-23 | 1996-01-25 | Merck Patent Gmbh | Ketotricyclo [5.2.1.0] decan-Derivate |
| DE4426216A1 (de) | 1994-07-23 | 1996-01-25 | Merck Patent Gmbh | Benzyliden-Norcampher-Derivate |
| US5665426A (en) | 1995-02-06 | 1997-09-09 | Kimberly-Clark Corporation | Soft treated tissue |
| DE19604744A1 (de) | 1996-02-09 | 1997-08-14 | Henkel Kgaa | Technische Di-/Triglyceridgemische |
| DE19623383C2 (de) * | 1996-06-12 | 1999-07-01 | Henkel Kgaa | Verwendung von Fettstoffen als Siliconersatz zur Herstellung von kosmetischen und/oder pharmazeutischen Zubereitungen |
| DE29724204U1 (de) * | 1996-06-12 | 2000-09-21 | Cognis Deutschland GmbH, 40589 Düsseldorf | Kosmetische und/oder pharmazeutische Zubereitungen |
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| EP1293504A3 (de) | 1996-07-08 | 2003-11-05 | Ciba SC Holding AG | Triazinderivate als UV-Filter in kosmetischen Mitteln |
| DE19712033A1 (de) | 1997-03-21 | 1998-09-24 | Basf Ag | Photostabile UV-Filter enthaltende kosmetische und pharmazeutische Zubereitungen |
| ES2246501T3 (es) | 1996-11-29 | 2006-02-16 | Basf Aktiengesellschaft | Preparados cosmeticos y farmaceuticos que contienen filtros uv-a fotoestables. |
| EP0884045A1 (en) * | 1997-06-06 | 1998-12-16 | Pfizer Products Inc. | Self-tanning dihydroxyacetone formulations having improved stability and providing enhanced delivery |
| JPH11106326A (ja) * | 1997-09-30 | 1999-04-20 | Nikko Chemical Co Ltd | 炭酸ジエステルを含有する外用剤又は化粧料 |
| DE19756377A1 (de) | 1997-12-18 | 1999-06-24 | Beiersdorf Ag | Verwendung von C¶1¶¶8¶-¶3¶¶8¶-Alkylhydroxystearoylstearat zur Verstärkung der UV-A-Schutzleistung kosmetischer oder dermatologischer Formulierungen |
| JP2000095662A (ja) * | 1998-09-24 | 2000-04-04 | Nisshin Oil Mills Ltd:The | 化粧料 |
| DE19858812A1 (de) | 1998-12-21 | 2000-06-29 | Cognis Deutschland Gmbh | Desodorierende kosmetische Mittel |
| US6153209A (en) | 1999-09-28 | 2000-11-28 | The Procter & Gamble Company | Article having a transferable breathable skin care composition thereon |
| EP1103246A1 (en) * | 1999-11-15 | 2001-05-30 | Cognis Corporation | Anhydrous powder compositions |
| DE19962877A1 (de) | 1999-12-24 | 2001-06-28 | Henkel Kgaa | Haut- und Haarpflegemittel |
| DE10002643A1 (de) | 2000-01-21 | 2001-07-26 | Cognis Deutschland Gmbh | Desodorierende Zubereitungen |
| DE10005018A1 (de) * | 2000-02-04 | 2001-08-09 | Henkel Kgaa | Deodorierende Haarpflegemittel |
| DE10014529A1 (de) | 2000-03-23 | 2001-09-27 | Cognis Deutschland Gmbh | Desodorierende Zubereitungen mit nanoskaligen Chitosanen und/oder Chitosanderivaten |
-
2000
- 2000-07-07 DE DE10033022A patent/DE10033022A1/de not_active Withdrawn
-
2001
- 2001-06-30 DE DE50109090T patent/DE50109090D1/de not_active Expired - Lifetime
- 2001-06-30 EP EP01962809A patent/EP1299074B1/de not_active Revoked
- 2001-06-30 AU AU2001295170A patent/AU2001295170A1/en not_active Abandoned
- 2001-06-30 ES ES01962809T patent/ES2259039T3/es not_active Expired - Lifetime
- 2001-06-30 US US10/332,286 patent/US7427406B2/en not_active Expired - Lifetime
- 2001-06-30 WO PCT/EP2001/007514 patent/WO2002003927A2/de not_active Ceased
- 2001-06-30 JP JP2002508383A patent/JP4909485B2/ja not_active Expired - Lifetime
- 2001-06-30 CN CN01812366A patent/CN1440271A/zh active Pending
- 2001-06-30 KR KR20037000227A patent/KR20030040349A/ko not_active Withdrawn
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