DMK ULTRASCREEN MINERAL SUNSCREEN- zinc oxide lotion
DMK Ultrascreen Mineral Sunscreen by
Drug Labeling and Warnings
DMK Ultrascreen Mineral Sunscreen by is a Otc medication manufactured, distributed, or labeled by Danne Montague King. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- DMK Ultrascreen Mineral Sunscreen
- DMK Ultrascreen Mineral Sunscreen
- DMK Ultrascreen Mineral Sunscreen
- DMK Ultrascreen Mineral Sunscreen
- DMK Ultrascreen Mineral Sunscreen
- DMK Ultrascreen Mineral Sunscreen
- DMK Ultrascreen Mineral Sunscreen
- DMK Ultrascreen Mineral Sunscreen
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INGREDIENTS AND APPEARANCE
DMK ULTRASCREEN MINERAL SUNSCREEN
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 81537-282 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 132 mg in 1 mL Inactive Ingredients Ingredient Name Strength PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) ISODODECANE (UNII: A8289P68Y2) .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) NIACINAMIDE (UNII: 25X51I8RD4) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB) PROPANEDIOL (UNII: 5965N8W85T) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) CARRAGEENAN (UNII: 5C69YCD2YJ) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) .BETA.-TOCOPHEROL (UNII: 9U6A490501) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 81537-282-02 1 in 1 CARTON 04/24/2025 1 NDC: 81537-282-01 65 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/24/2025 Labeler - Danne Montague King (624242264)
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