Country: United States
Language: English
Source: NLM (National Library of Medicine)
Octinoxate 7.5%, Octisalate 5.0%, Oxybenzone 3.0%
PHARMAGEL INTERNATIONAL INC
TOPICAL
OTC DRUG
Sunscreen Lightens the appearance of age spots & skin discoloration. Provides moderate protections against sunburn.
OTC monograph not final
DERMA FADE- OCTINOXATE, OCTISALATE, OXYBENZONE CREAM PHARMAGEL INTERNATIONAL INC ---------- PHARMAGEL - DERMA FADE (67879-301) ACTIVE INGREDIENTS Octinoxate 7.5% Octisalate 5.0% Oxybenzone 3.0% PURPOSE Sunscreen USES Lightens the appearance of age spots & skin discoloration. Provides moderate protections against sunburn. WARNINGS Warnings using this product – For external use only. Avoid contact with eyes. If product gets into the eyes, rinse thoroughly with water. Do not use on children under 12 years of age unless directed by a doctor. Stop use & consult a doctor if rash or irritation develops and persists. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. DIRECTIONS Apply to age spots and skin discoloration. Can be used as a full face moisturizing treatment and sunscreen before sun exposure. INACTIVE INGREDIENTS: ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALLANTOIN, BIOTIN, BUTYLENE GLYCOL, CAMELLIA SINENSIS (GREEN TEA) LEAF EXTRACT, CAPRYLYL GLYCOL, CETEARYL ALCOHOL, CITRIC ACID, CITRUS UNSHIU PEEL EXTRACT, CYPERUS ROTUNDUS ROOT EXTRACT, DIMETHICONE, DISODIUM EDTA, ETHYLHEXYL PALMITATE, ETHYLHEXYLGLYCERIN, FRAGRANCE (PARFUM), GLYCERIN, GLYCERYL STEARATE, GLYCOLIC ACID, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, HEXYLENE GLYCOL, HYDROXYETHYLCELLULOSE, KOJIC ACID, LACTIC ACID, MAGNESIUM ASCORBYL PHOSPHATE, MORUS ALBA LEAF EXTRACT, MYRISTYL LAURATE, MYRISTYL MYRISTATE, NIACIN, PANTHENOL, PEG-100 STEARATE, PHENOXYETHANOL, PHYLLANTHUS EMBLICA FRUIT EXRACT, PROPYLENE GLYCOL, RED 40 (CI 16035), SODIUM CITRATE, STEARIC ACID, TETRASODIUM EDTA, TRIETHANOLAMINE, UNDECYLENIC ACID, UNDECYLENOYL PHENYLALANINE, WATER (AQUA), YELLOW 6 (CI 15985) DERMA FADE octinoxate, octisalate, oxybenzone cream PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:67879-301 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in Read the complete document