Label: SUNSCREEN- zinc oxide sunscreen ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 62932-253-47 - Packager: Private Label Select Ltd CO
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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Drug Label Information
Updated January 4, 2022
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- ARTWORK
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INGREDIENTS AND APPEARANCE
SUNSCREEN
zinc oxide sunscreen ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62932-253 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 25 g in 100 g Inactive Ingredients Ingredient Name Strength WHITE WAX (UNII: 7G1J5DA97F) .BETA.-TOCOPHEROL (UNII: 9U6A490501) SUNFLOWER OIL (UNII: 3W1JG795YI) CASTOR OIL (UNII: D5340Y2I9G) RASPBERRY SEED OIL (UNII: 9S8867952A) APRICOT KERNEL OIL (UNII: 54JB35T06A) .GAMMA.-TOCOPHEROL (UNII: 8EF1Z1238F) COCONUT OIL (UNII: Q9L0O73W7L) SHEA BUTTER (UNII: K49155WL9Y) ARGAN OIL (UNII: 4V59G5UW9X) ROSA CANINA SEED (UNII: 4503R1M9UT) .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9) .DELTA.-TOCOPHEROL (UNII: JU84X1II0N) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62932-253-47 85 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 01/01/2020 Labeler - Private Label Select Ltd CO (005415463)
