- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- STOP USE
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Other Ingredients
Water (Aqua), Octyldodecyl Neopentanoate, C12-15 Alkyl Benzoate, BUtyrosermum Parkii (Shea Butter), Glyceryl Stearate, Undecylenoyl phenylalanine, Caprylic/Capric Triglyceride, Cetyl Alcohol, PEG-100 Stearate, Silica, Glycerin, Triethanolamine, Polyglyceryl-3 Laurate, Tocopheryl Acetate,Steareth-20, Tetrahexyldecyl Ascorbate, Ceteth-20, Mel {honey extract}, Diethylhexyl Syringylidenemalonate, Sodium Palmitoyl Proline, Nymphaea Alba Flower Extract,, Camellia Sinensis Leaf Extract, Citrus Unshiu Peel Extract, Butylene Glycol, Carbomer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance (Parfum), Phenoxyethanol, Disodium EDTA, Chlorphenesin, Benzoic Acid, Sorbic Acid, Caramel.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DAILY FADE SPF15
sunscreen creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59735-306 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 2 g in 100 g Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 5 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59735-306-56 1 in 1 CARTON 1 56 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 03/06/2006 Labeler - Biocosetic Research Labs (078870292)