Label: SUNSCREEN- zinc oxide sunscreen stick
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Contains inactivated NDC Code(s)
NDC Code(s): 62932-173-26 - Packager: Private Label Select Ltd CO
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 15, 2020
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INGREDIENTS AND APPEARANCE
SUNSCREEN
zinc oxide sunscreen stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62932-173 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 22 g in 100 g Inactive Ingredients Ingredient Name Strength .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF) SUNFLOWER OIL (UNII: 3W1JG795YI) WHITE WAX (UNII: 7G1J5DA97F) SHEA BUTTER (UNII: K49155WL9Y) ALOE VERA LEAF (UNII: ZY81Z83H0X) COCONUT OIL (UNII: Q9L0O73W7L) GERANIOL (UNII: L837108USY) CITRUS SINENSIS FLOWER OIL (UNII: AJ56JP5TFP) TOCOPHEROL (UNII: R0ZB2556P8) CANDELILLA WAX (UNII: WL0328HX19) CARNAUBA WAX (UNII: R12CBM0EIZ) CASTOR OIL (UNII: D5340Y2I9G) COCOA BUTTER (UNII: 512OYT1CRR) LINALOOL, (+/-)- (UNII: D81QY6I88E) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62932-173-26 22 g in 1 TUBE; Type 0: Not a Combination Product 12/31/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 12/31/2018 Labeler - Private Label Select Ltd CO (005415463) Registrant - Private Label Select Ltd CO (005415463)