MXPA06009174A - Composiciones para el cuidado de la piel. - Google Patents
Composiciones para el cuidado de la piel.Info
- Publication number
- MXPA06009174A MXPA06009174A MXPA06009174A MXPA06009174A MXPA06009174A MX PA06009174 A MXPA06009174 A MX PA06009174A MX PA06009174 A MXPA06009174 A MX PA06009174A MX PA06009174 A MXPA06009174 A MX PA06009174A MX PA06009174 A MXPA06009174 A MX PA06009174A
- Authority
- MX
- Mexico
- Prior art keywords
- composition according
- composition
- copolymer
- salt
- acid
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 176
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims abstract description 98
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims abstract description 49
- 229960004889 salicylic acid Drugs 0.000 claims abstract description 49
- 229920001577 copolymer Polymers 0.000 claims abstract description 48
- 150000003839 salts Chemical class 0.000 claims abstract description 39
- 239000003349 gelling agent Substances 0.000 claims abstract description 30
- 239000002253 acid Substances 0.000 claims abstract description 18
- 239000006185 dispersion Substances 0.000 claims abstract description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 34
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 239000006184 cosolvent Substances 0.000 claims description 17
- 229960002163 hydrogen peroxide Drugs 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 15
- BQMNFPBUAQPINY-UHFFFAOYSA-N azane;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonic acid Chemical compound [NH4+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C BQMNFPBUAQPINY-UHFFFAOYSA-N 0.000 claims description 14
- -1 lomefloxacin Chemical class 0.000 claims description 14
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 11
- 239000000758 substrate Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000002562 thickening agent Substances 0.000 claims description 9
- 239000004480 active ingredient Substances 0.000 claims description 7
- 239000003242 anti bacterial agent Substances 0.000 claims description 6
- 150000002978 peroxides Chemical class 0.000 claims description 6
- 239000000230 xanthan gum Substances 0.000 claims description 6
- 229920001285 xanthan gum Polymers 0.000 claims description 6
- 235000010493 xanthan gum Nutrition 0.000 claims description 6
- 229940082509 xanthan gum Drugs 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000006071 cream Substances 0.000 claims description 5
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 5
- 244000144927 Aloe barbadensis Species 0.000 claims description 4
- 235000002961 Aloe barbadensis Nutrition 0.000 claims description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 claims description 4
- 235000011399 aloe vera Nutrition 0.000 claims description 4
- 230000000844 anti-bacterial effect Effects 0.000 claims description 4
- 239000001913 cellulose Substances 0.000 claims description 4
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 229920000742 Cotton Polymers 0.000 claims description 3
- 241000124033 Salix Species 0.000 claims description 3
- 230000000840 anti-viral effect Effects 0.000 claims description 3
- CRDAMVZIKSXKFV-FBXUGWQNSA-N (2-cis,6-cis)-farnesol Chemical compound CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 claims description 2
- 239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 claims description 2
- SGKRLCUYIXIAHR-AKNGSSGZSA-N (4s,4ar,5s,5ar,6r,12ar)-4-(dimethylamino)-1,5,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1=CC=C2[C@H](C)[C@@H]([C@H](O)[C@@H]3[C@](C(O)=C(C(N)=O)C(=O)[C@H]3N(C)C)(O)C3=O)C3=C(O)C2=C1O SGKRLCUYIXIAHR-AKNGSSGZSA-N 0.000 claims description 2
- FFTVPQUHLQBXQZ-KVUCHLLUSA-N (4s,4as,5ar,12ar)-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1C2=C(N(C)C)C=CC(O)=C2C(O)=C2[C@@H]1C[C@H]1[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]1(O)C2=O FFTVPQUHLQBXQZ-KVUCHLLUSA-N 0.000 claims description 2
- AFNXATANNDIXLG-SFHVURJKSA-N 1-[(2r)-2-[(4-chlorophenyl)methylsulfanyl]-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound C1=CC(Cl)=CC=C1CS[C@H](C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 AFNXATANNDIXLG-SFHVURJKSA-N 0.000 claims description 2
- MCCACAIVAXEFAL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]imidazole;nitric acid Chemical compound O[N+]([O-])=O.ClC1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 MCCACAIVAXEFAL-UHFFFAOYSA-N 0.000 claims description 2
- LEZWWPYKPKIXLL-UHFFFAOYSA-N 1-{2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl}imidazole Chemical compound C1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 LEZWWPYKPKIXLL-UHFFFAOYSA-N 0.000 claims description 2
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 claims description 2
- UAPFFXGASFVGHS-UHFFFAOYSA-N 2,2-dimethyl-3-oxopent-4-enoic acid Chemical compound OC(=O)C(C)(C)C(=O)C=C UAPFFXGASFVGHS-UHFFFAOYSA-N 0.000 claims description 2
- SUMAWDZJEIQACJ-UHFFFAOYSA-N 2-methylpyridine-4-carbaldehyde Chemical compound CC1=CC(C=O)=CC=N1 SUMAWDZJEIQACJ-UHFFFAOYSA-N 0.000 claims description 2
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 claims description 2
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 claims description 2
- 108010001478 Bacitracin Proteins 0.000 claims description 2
- 239000004342 Benzoyl peroxide Substances 0.000 claims description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- 229920003043 Cellulose fiber Polymers 0.000 claims description 2
- 229930186147 Cephalosporin Natural products 0.000 claims description 2
- MUQNGPZZQDCDFT-JNQJZLCISA-N Halcinonide Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CCl)[C@@]1(C)C[C@@H]2O MUQNGPZZQDCDFT-JNQJZLCISA-N 0.000 claims description 2
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 claims description 2
- CMWTZPSULFXXJA-UHFFFAOYSA-N Naproxen Natural products C1=C(C(C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-UHFFFAOYSA-N 0.000 claims description 2
- 229930193140 Neomycin Natural products 0.000 claims description 2
- JNTOCHDNEULJHD-UHFFFAOYSA-N Penciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(CCC(CO)CO)C=N2 JNTOCHDNEULJHD-UHFFFAOYSA-N 0.000 claims description 2
- 229930182555 Penicillin Natural products 0.000 claims description 2
- 108010040201 Polymyxins Proteins 0.000 claims description 2
- 239000004098 Tetracycline Substances 0.000 claims description 2
- 229960001138 acetylsalicylic acid Drugs 0.000 claims description 2
- 229960004150 aciclovir Drugs 0.000 claims description 2
- MKUXAQIIEYXACX-UHFFFAOYSA-N aciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 claims description 2
- 229960000458 allantoin Drugs 0.000 claims description 2
- 150000003863 ammonium salts Chemical group 0.000 claims description 2
- 230000000843 anti-fungal effect Effects 0.000 claims description 2
- 230000003110 anti-inflammatory effect Effects 0.000 claims description 2
- 230000000845 anti-microbial effect Effects 0.000 claims description 2
- 229940121375 antifungal agent Drugs 0.000 claims description 2
- 229960003071 bacitracin Drugs 0.000 claims description 2
- 229930184125 bacitracin Natural products 0.000 claims description 2
- CLKOFPXJLQSYAH-ABRJDSQDSA-N bacitracin A Chemical compound C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2N=CNC=2)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 CLKOFPXJLQSYAH-ABRJDSQDSA-N 0.000 claims description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 2
- 229960001102 betamethasone dipropionate Drugs 0.000 claims description 2
- CIWBQSYVNNPZIQ-XYWKZLDCSA-N betamethasone dipropionate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)COC(=O)CC)(OC(=O)CC)[C@@]1(C)C[C@@H]2O CIWBQSYVNNPZIQ-XYWKZLDCSA-N 0.000 claims description 2
- 229960004311 betamethasone valerate Drugs 0.000 claims description 2
- SNHRLVCMMWUAJD-SUYDQAKGSA-N betamethasone valerate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CO)(OC(=O)CCCC)[C@@]1(C)C[C@@H]2O SNHRLVCMMWUAJD-SUYDQAKGSA-N 0.000 claims description 2
- 229960003273 butenafine hydrochloride Drugs 0.000 claims description 2
- 239000011575 calcium Substances 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 229940118258 calcium undecylenate Drugs 0.000 claims description 2
- KHAVLLBUVKBTBG-UHFFFAOYSA-N caproleic acid Natural products OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 229940106164 cephalexin Drugs 0.000 claims description 2
- ZAIPMKNFIOOWCQ-UEKVPHQBSA-N cephalexin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)C)C(O)=O)=CC=CC=C1 ZAIPMKNFIOOWCQ-UEKVPHQBSA-N 0.000 claims description 2
- 229940124587 cephalosporin Drugs 0.000 claims description 2
- 150000001780 cephalosporins Chemical class 0.000 claims description 2
- SCKYRAXSEDYPSA-UHFFFAOYSA-N ciclopirox Chemical compound ON1C(=O)C=C(C)C=C1C1CCCCC1 SCKYRAXSEDYPSA-UHFFFAOYSA-N 0.000 claims description 2
- 229960002227 clindamycin Drugs 0.000 claims description 2
- KDLRVYVGXIQJDK-AWPVFWJPSA-N clindamycin Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](SC)O1 KDLRVYVGXIQJDK-AWPVFWJPSA-N 0.000 claims description 2
- 229960004703 clobetasol propionate Drugs 0.000 claims description 2
- CBGUOGMQLZIXBE-XGQKBEPLSA-N clobetasol propionate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CCl)(OC(=O)CC)[C@@]1(C)C[C@@H]2O CBGUOGMQLZIXBE-XGQKBEPLSA-N 0.000 claims description 2
- 229960004022 clotrimazole Drugs 0.000 claims description 2
- VNFPBHJOKIVQEB-UHFFFAOYSA-N clotrimazole Chemical compound ClC1=CC=CC=C1C(N1C=NC=C1)(C=1C=CC=CC=1)C1=CC=CC=C1 VNFPBHJOKIVQEB-UHFFFAOYSA-N 0.000 claims description 2
- 229960003722 doxycycline Drugs 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 229960003913 econazole Drugs 0.000 claims description 2
- 229940043259 farnesol Drugs 0.000 claims description 2
- 229930002886 farnesol Natural products 0.000 claims description 2
- RFHAOTPXVQNOHP-UHFFFAOYSA-N fluconazole Chemical compound C1=NC=NN1CC(C=1C(=CC(F)=CC=1)F)(O)CN1C=NC=N1 RFHAOTPXVQNOHP-UHFFFAOYSA-N 0.000 claims description 2
- 229960004884 fluconazole Drugs 0.000 claims description 2
- 229960001347 fluocinolone acetonide Drugs 0.000 claims description 2
- FEBLZLNTKCEFIT-VSXGLTOVSA-N fluocinolone acetonide Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@]1(F)[C@@H]2[C@@H]2C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]2(C)C[C@@H]1O FEBLZLNTKCEFIT-VSXGLTOVSA-N 0.000 claims description 2
- 229960002383 halcinonide Drugs 0.000 claims description 2
- 229960000890 hydrocortisone Drugs 0.000 claims description 2
- 229960001680 ibuprofen Drugs 0.000 claims description 2
- DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 claims description 2
- 229960000991 ketoprofen Drugs 0.000 claims description 2
- 229940069445 licorice extract Drugs 0.000 claims description 2
- ZEKZLJVOYLTDKK-UHFFFAOYSA-N lomefloxacin Chemical compound FC1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNC(C)C1 ZEKZLJVOYLTDKK-UHFFFAOYSA-N 0.000 claims description 2
- 229960002422 lomefloxacin Drugs 0.000 claims description 2
- 229960000282 metronidazole Drugs 0.000 claims description 2
- VAOCPAMSLUNLGC-UHFFFAOYSA-N metronidazole Chemical compound CC1=NC=C([N+]([O-])=O)N1CCO VAOCPAMSLUNLGC-UHFFFAOYSA-N 0.000 claims description 2
- 229960005040 miconazole nitrate Drugs 0.000 claims description 2
- 229960004023 minocycline Drugs 0.000 claims description 2
- 229960002009 naproxen Drugs 0.000 claims description 2
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical compound C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 claims description 2
- 229960004927 neomycin Drugs 0.000 claims description 2
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims description 2
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 claims description 2
- 229960000988 nystatin Drugs 0.000 claims description 2
- VQOXZBDYSJBXMA-NQTDYLQESA-N nystatin A1 Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/CC/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 VQOXZBDYSJBXMA-NQTDYLQESA-N 0.000 claims description 2
- 239000007764 o/w emulsion Substances 0.000 claims description 2
- 229960003752 oseltamivir Drugs 0.000 claims description 2
- VSZGPKBBMSAYNT-RRFJBIMHSA-N oseltamivir Chemical compound CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1 VSZGPKBBMSAYNT-RRFJBIMHSA-N 0.000 claims description 2
- 229960001179 penciclovir Drugs 0.000 claims description 2
- 150000002960 penicillins Chemical class 0.000 claims description 2
- 150000007660 quinolones Chemical class 0.000 claims description 2
- 150000003431 steroids Chemical class 0.000 claims description 2
- 229960002607 sulconazole Drugs 0.000 claims description 2
- SKIVFJLNDNKQPD-UHFFFAOYSA-N sulfacetamide Chemical compound CC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 SKIVFJLNDNKQPD-UHFFFAOYSA-N 0.000 claims description 2
- 229960002673 sulfacetamide Drugs 0.000 claims description 2
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 claims description 2
- 229960000699 terbinafine hydrochloride Drugs 0.000 claims description 2
- 235000019364 tetracycline Nutrition 0.000 claims description 2
- 150000003522 tetracyclines Chemical class 0.000 claims description 2
- 229940040944 tetracyclines Drugs 0.000 claims description 2
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 claims description 2
- 229960002117 triamcinolone acetonide Drugs 0.000 claims description 2
- YNDXUCZADRHECN-JNQJZLCISA-N triamcinolone acetonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O YNDXUCZADRHECN-JNQJZLCISA-N 0.000 claims description 2
- 229960000497 trovafloxacin Drugs 0.000 claims description 2
- WVPSKSLAZQPAKQ-CDMJZVDBSA-N trovafloxacin Chemical compound C([C@H]1[C@@H]([C@H]1C1)N)N1C(C(=CC=1C(=O)C(C(O)=O)=C2)F)=NC=1N2C1=CC=C(F)C=C1F WVPSKSLAZQPAKQ-CDMJZVDBSA-N 0.000 claims description 2
- 229950008396 ulobetasol propionate Drugs 0.000 claims description 2
- BDSYKGHYMJNPAB-LICBFIPMSA-N ulobetasol propionate Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@]1(F)[C@@H]2[C@@H]2C[C@H](C)[C@@](C(=O)CCl)(OC(=O)CC)[C@@]2(C)C[C@@H]1O BDSYKGHYMJNPAB-LICBFIPMSA-N 0.000 claims description 2
- GAAKLDANOSASAM-UHFFFAOYSA-N undec-10-enoic acid;zinc Chemical compound [Zn].OC(=O)CCCCCCCCC=C GAAKLDANOSASAM-UHFFFAOYSA-N 0.000 claims description 2
- 229960002703 undecylenic acid Drugs 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229940118257 zinc undecylenate Drugs 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- KIOWXTOCDZJCBM-UHFFFAOYSA-N 2-docosoxyethyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCOCCOC(=O)C(C)=C KIOWXTOCDZJCBM-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N acetaldehyde dimethyl acetal Natural products COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 claims 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims 1
- 229940110830 beheneth-25 methacrylate Drugs 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 206010000496 acne Diseases 0.000 abstract description 11
- 208000002874 Acne Vulgaris Diseases 0.000 abstract description 10
- 238000011282 treatment Methods 0.000 abstract description 4
- 230000000699 topical effect Effects 0.000 abstract description 3
- 230000000069 prophylactic effect Effects 0.000 abstract 1
- 230000000246 remedial effect Effects 0.000 abstract 1
- 239000000499 gel Substances 0.000 description 43
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
- 239000004615 ingredient Substances 0.000 description 19
- 238000000034 method Methods 0.000 description 13
- 239000003995 emulsifying agent Substances 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- 239000002304 perfume Substances 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 9
- 229940113096 isoceteth 20 Drugs 0.000 description 9
- 239000000463 material Substances 0.000 description 9
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Landscapes
- 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)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Dispersion Chemistry (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0403702.4A GB0403702D0 (en) | 2004-02-19 | 2004-02-19 | Skincare compositions |
| PCT/GB2005/000524 WO2005079746A1 (en) | 2004-02-19 | 2005-02-15 | Skincare compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA06009174A true MXPA06009174A (es) | 2007-01-26 |
Family
ID=32040021
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA06009174A MXPA06009174A (es) | 2004-02-19 | 2005-02-15 | Composiciones para el cuidado de la piel. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20070140993A1 (https=) |
| EP (1) | EP1722749B1 (https=) |
| JP (1) | JP2007523138A (https=) |
| CN (2) | CN1937997A (https=) |
| AT (1) | ATE398995T1 (https=) |
| AU (1) | AU2005215214B2 (https=) |
| BR (1) | BRPI0507727A (https=) |
| CA (1) | CA2556815C (https=) |
| DE (1) | DE602005007711D1 (https=) |
| ES (1) | ES2308440T3 (https=) |
| GB (1) | GB0403702D0 (https=) |
| MX (1) | MXPA06009174A (https=) |
| RU (1) | RU2006133380A (https=) |
| WO (1) | WO2005079746A1 (https=) |
| ZA (1) | ZA200606317B (https=) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006080992A1 (en) * | 2005-01-25 | 2006-08-03 | Howard Murad | Fragrance delivery system |
| US20070065385A1 (en) * | 2005-09-19 | 2007-03-22 | Clariant International, Ltd. | Cold production method for pearly lustre preparations containing alcohols |
| FR2905595B1 (fr) * | 2006-09-08 | 2008-10-31 | Oreal | Gel hydroalcoolique |
| CA2708534C (en) * | 2007-12-17 | 2015-12-15 | Novapharm Research (Australia) Pty Ltd | Non-staining bactericidal, fungicidal and viricidal compositions |
| DE102007061970A1 (de) * | 2007-12-21 | 2008-07-03 | Clariant International Limited | Kosmetische, pharmazeutische oder dermatologische Zusammensetzungen enthaltend einen hohen Gehalt an wasserlöslichen Pflegekomponenten |
| EP2262469A4 (en) * | 2008-04-15 | 2013-12-04 | Immanence Integrale Dermo Correction Inc | SKIN CARE COMPOSITIONS AND METHOD FOR THEIR USE |
| CN102056481A (zh) * | 2008-06-05 | 2011-05-11 | 陶氏制药科学公司 | 包含低浓度的在水和水混溶性有机溶剂中的悬浮液形式的过氧苯甲酰的局部药物制剂 |
| US20100105750A1 (en) * | 2008-10-23 | 2010-04-29 | Nycomed Us Inc. | Stable metronidazole gel formulations |
| ES2637447T3 (es) | 2009-08-31 | 2017-10-13 | Dr. Reddy's Laboratories Ltd. | Formulaciones tópicas que contienen un esteroide |
| US20110236503A1 (en) * | 2010-03-23 | 2011-09-29 | Cosmalabs International, Llc | Topical Skincare Composition |
| EP2632578A4 (en) * | 2010-10-29 | 2014-12-03 | Msd Consumer Care Inc | CONCENTRATED THERAPEUTIC SOLUTION |
| FR2969921B1 (fr) * | 2011-01-05 | 2013-08-09 | Oreal | Produit cosmetique en deux parties |
| FR2980691B1 (fr) * | 2011-09-30 | 2014-03-14 | Galderma Sa | Composition de lavage |
| JP2014524901A (ja) | 2011-06-13 | 2014-09-25 | ザ プロクター アンド ギャンブル カンパニー | ジアミドゲル化剤を含むパーソナルケア組成物及び使用方法 |
| WO2012174091A2 (en) | 2011-06-13 | 2012-12-20 | The Procter & Gamble Company | PERSONAL CARE COMPOSITIONS COMPRISING A pH TUNEABLE GELLANT AND METHODS OF USING |
| WO2012177757A2 (en) | 2011-06-20 | 2012-12-27 | The Procter & Gamble Company | Personal care compositions comprising shaped abrasive particles |
| JP2013116870A (ja) * | 2011-12-02 | 2013-06-13 | Rohto Pharmaceutical Co Ltd | 皮膚外用組成物 |
| US9271912B2 (en) | 2012-06-13 | 2016-03-01 | The Procter & Gamble Company | Personal care compositions comprising a pH tuneable gellant and methods of using |
| FR2993466B1 (fr) * | 2012-07-18 | 2014-08-15 | Prevor Internat | Utilisation d'une creme de protection contre les effets des agents chimiques agressifs en contact avec la peau |
| JP6009373B2 (ja) * | 2013-02-28 | 2016-10-19 | 日本メナード化粧品株式会社 | 水中油型粉末化粧料 |
| TWI663982B (zh) * | 2013-09-03 | 2019-07-01 | 合一生技股份有限公司 | 到手香萃取物用於製備具抗微生物功效組合物之用途 |
| CN103462843A (zh) * | 2013-09-11 | 2013-12-25 | 拉芳家化股份有限公司 | 一种温和护肤凝胶 |
| JP6279457B2 (ja) * | 2013-11-19 | 2018-02-14 | 株式会社 資生堂 | 水中油型乳化化粧料 |
| JP6592233B2 (ja) * | 2013-12-25 | 2019-10-16 | ロート製薬株式会社 | 皮膚外用組成物 |
| US20160184431A1 (en) * | 2014-03-11 | 2016-06-30 | Promius Pharma Llc | Topical compositions comprising a corticosteroid |
| EP3261619A4 (en) | 2015-02-25 | 2018-10-24 | Sun Pharma Advanced Research Company Ltd | Nanoparticulate composition |
| US11364183B2 (en) | 2018-04-30 | 2022-06-21 | L'oréal | Cosmetic system containing an applicator and a gel composition |
| US20210196589A1 (en) * | 2019-12-26 | 2021-07-01 | L'oreal | Compositions, dispensing systems and methods for providing sensorial and aesthetic benefits to acne prone skin |
| US20210196591A1 (en) * | 2019-12-26 | 2021-07-01 | L'oreal | Nature-based compositions, dispensing systems and methods for providing sensorial and aesthetic benefits to acne prone skin |
| DE112023001807T5 (de) | 2022-03-31 | 2025-01-23 | Galderma Holding SA | Körperpflegezusammensetzungen für empfindliche Haut und Anwendungsmethoden |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58198421A (ja) * | 1982-05-14 | 1983-11-18 | Reiko Kosaka | 皮膚脱色及び皮膚疾患治療用組成物 |
| WO1993010756A1 (en) * | 1991-11-25 | 1993-06-10 | Richardson-Vicks, Inc. | Use of salicylic acid for regulating skin wrinkles and/or skin atrophy |
| AU1438295A (en) * | 1993-12-17 | 1995-07-03 | Albert M. Kligman | Method for treatment of papulo-pustules and comedones of the skin |
| US5693318A (en) * | 1996-07-15 | 1997-12-02 | Basf Corporation | Stable salicylic acid and peroxide containing skin and hair cleanser composition |
| US5736582A (en) * | 1996-10-10 | 1998-04-07 | Devillez; Richard L. | Method and composition for controlled delivery of nascent oxygen from hydrogen peroxide source for skin treatment |
| KR20010013377A (ko) * | 1997-06-04 | 2001-02-26 | 데이비드 엠 모이어 | 마일드한 잔류성 항균 조성물 |
| US6071541A (en) * | 1998-07-31 | 2000-06-06 | Murad; Howard | Pharmaceutical compositions and methods for managing skin conditions |
| DE10000648A1 (de) * | 2000-01-11 | 2001-07-12 | Clariant Gmbh | Wasserlösliche oder wasserquellbare vernetzte Copolymere |
| JP4764588B2 (ja) * | 2000-02-22 | 2011-09-07 | カラー アクセス，インコーポレイティド | ゲル化された水性化粧品組成物 |
| US20020031556A1 (en) * | 2000-07-21 | 2002-03-14 | Lindahl Ake R. | Stabilized hydrogen peroxide composition and method of making a stabilized hydrogen peroxide composition |
| DE10059824A1 (de) * | 2000-12-01 | 2002-06-13 | Clariant Gmbh | Elektrolythaltige kosmetische, pharmazeutische und dermatologische Mittel |
| DE10059822A1 (de) * | 2000-12-01 | 2002-06-13 | Clariant Gmbh | Saure kosmetische, pharmazeutische und dermatologische Mittel |
| US6428772B1 (en) * | 2001-06-25 | 2002-08-06 | Blistex Inc. | Acne treatment composition with cooling effect |
| US6986895B2 (en) * | 2001-09-12 | 2006-01-17 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Thickened cosmetic compositions |
| US20030118620A1 (en) * | 2001-09-12 | 2003-06-26 | Unilever Home & Personal Care Usa, Division Of Conopco Inc. | Thickener system for cosmetic compositions |
| EP1670424A2 (en) * | 2003-09-13 | 2006-06-21 | Boots Healthcare International Limited | Skincare compositions comprising salicylic acid |
-
2004
- 2004-02-19 GB GBGB0403702.4A patent/GB0403702D0/en not_active Ceased
-
2005
- 2005-02-15 US US10/590,060 patent/US20070140993A1/en not_active Abandoned
- 2005-02-15 ES ES05708342T patent/ES2308440T3/es not_active Expired - Lifetime
- 2005-02-15 AU AU2005215214A patent/AU2005215214B2/en not_active Ceased
- 2005-02-15 EP EP05708342A patent/EP1722749B1/en not_active Revoked
- 2005-02-15 BR BRPI0507727-3A patent/BRPI0507727A/pt not_active Application Discontinuation
- 2005-02-15 WO PCT/GB2005/000524 patent/WO2005079746A1/en not_active Ceased
- 2005-02-15 MX MXPA06009174A patent/MXPA06009174A/es not_active Application Discontinuation
- 2005-02-15 DE DE602005007711T patent/DE602005007711D1/de not_active Expired - Lifetime
- 2005-02-15 AT AT05708342T patent/ATE398995T1/de not_active IP Right Cessation
- 2005-02-15 JP JP2006553648A patent/JP2007523138A/ja active Pending
- 2005-02-15 CN CNA2005800054053A patent/CN1937997A/zh active Pending
- 2005-02-15 CA CA2556815A patent/CA2556815C/en not_active Expired - Fee Related
- 2005-02-15 RU RU2006133380/15A patent/RU2006133380A/ru not_active Application Discontinuation
- 2005-02-19 CN CNA2005800111376A patent/CN1942164A/zh active Pending
-
2006
- 2006-07-31 ZA ZA200606317A patent/ZA200606317B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2007523138A (ja) | 2007-08-16 |
| RU2006133380A (ru) | 2008-03-27 |
| GB0403702D0 (en) | 2004-03-24 |
| ES2308440T3 (es) | 2008-12-01 |
| WO2005079746A1 (en) | 2005-09-01 |
| CN1942164A (zh) | 2007-04-04 |
| CA2556815A1 (en) | 2005-09-01 |
| ZA200606317B (en) | 2008-02-27 |
| EP1722749A1 (en) | 2006-11-22 |
| AU2005215214B2 (en) | 2011-06-23 |
| BRPI0507727A (pt) | 2007-07-10 |
| ATE398995T1 (de) | 2008-07-15 |
| CA2556815C (en) | 2012-11-27 |
| AU2005215214A1 (en) | 2005-09-01 |
| CN1937997A (zh) | 2007-03-28 |
| EP1722749B1 (en) | 2008-06-25 |
| US20070140993A1 (en) | 2007-06-21 |
| DE602005007711D1 (de) | 2008-08-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |