Label: MINERAL FOUNDATION SPF 30-3W- zinc oxide and titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 62742-4097-1, 62742-4097-2 - Packager: Allure Labs Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 5, 2017
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INGREDIENTS AND APPEARANCE
MINERAL FOUNDATION SPF 30-3W
zinc oxide and titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4097 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 55 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 44 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) PERFLUNAFENE (UNII: 54A06VV62N) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E) MAGNESIUM SILICATE (UNII: 9B9691B2N9) NYLON-12 (UNII: 446U8J075B) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SANDALWOOD (UNII: 3641YW25N2) PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G) BARLEY (UNII: 5PWM7YLI7R) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S) CENTELLA ASIATICA (UNII: 7M867G6T1U) CETEARYL OLIVATE (UNII: 58B69Q84JO) SORBITAN OLIVATE (UNII: MDL271E3GR) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) STEARIC ACID (UNII: 4ELV7Z65AP) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) HEXYL LAURATE (UNII: 4CG9F9W01Q) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4097-2 1 in 1 CARTON 12/05/2017 1 NDC:62742-4097-1 29.6 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 11/29/2017 Labeler - Allure Labs Inc. (926831603)