Label: POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 COCADA- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 CAPUCCINO- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 MANJAR- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 MOCHA- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 COCOA- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 CREMA- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 FLAN- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 ALFAJOR- octinoxate powder
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 WAFFLE- octinoxate powder
-
Contains inactivated NDC Code(s)
NDC Code(s): 43596-0854-1, 43596-0855-1, 43596-0856-1, 43596-0857-1, view more43596-0858-1, 43596-0859-1, 43596-0860-1, 43596-0861-1, 43596-0862-1 - Packager: Ventura Corporation LTD
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 2, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
Warnings
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn not skin cancer or early skin aging.
Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove
For external use only - DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
Inactive ingredients: mica, talc, zinc stearate, methyl methacrylate crosspolymer, boron nitride, dimethicone, octyldodecanol, trimethylsiloxysilicate, perfluorooctyl triethoxysilane, tocopheryl acetate, magnesium myristate, phenoxyethanol, caprylyl glycol, fragrance, chlorphenesin, benzyl alcohol, linalool, hexyl cinnamal, limonene. May Contain: titanium dioxide, iron oxides.
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 COCADA
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0858 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0858-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 CAPUCCINO
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0859 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0859-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 MANJAR
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0860 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0860-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 MOCHA
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0861 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0861-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 COCOA
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0862 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0862-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 CREMA
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0854 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) OCTYLDODECANOL (UNII: 461N1O614Y) CHLORPHENESIN (UNII: I670DAL4SZ) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0854-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 FLAN
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0855 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0855-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 ALFAJOR
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0856 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0856-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 POLVOS COMPACTOS DE ALTA COBERTURA CON FPS 20 WAFFLE
octinoxate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43596-0857 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) FERRIC OXIDE RED (UNII: 1K09F3G675) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) DIMETHICONE (UNII: 92RU3N3Y1O) TALC (UNII: 7SEV7J4R1U) ZINC STEARATE (UNII: H92E6QA4FV) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PERFLUOROOCTYL TRIETHOXYSILANE (UNII: 814P46684U) MAGNESIUM MYRISTATE (UNII: Z1917F0578) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTYLDODECANOL (UNII: 461N1O614Y) MICA (UNII: V8A1AW0880) BORON NITRIDE (UNII: 2U4T60A6YD) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43596-0857-1 7 g in 1 CARTON; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/01/2020 Labeler - Ventura Corporation LTD (602751344) Establishment Name Address ID/FEI Business Operations BEL STAR S A 880160197 manufacture(43596-0854, 43596-0855, 43596-0856, 43596-0857, 43596-0858, 43596-0859, 43596-0860, 43596-0861, 43596-0862)