Label: FACIAL SUNSCREEN cream
- NDC Code(s): 84067-949-01
- Packager: Shantou Youjia E-Commerce Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated April 19, 2024
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INGREDIENTS AND APPEARANCE
FACIAL SUNSCREEN
facial sunscreen creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84067-949 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 10 mg in 50 g HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID 12.5 mg in 50 g TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8) TOCOPHEROL 2.5 mg in 50 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 10 mg in 50 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 15 mL in 50 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84067-949-01 50 g in 1 TUBE; Type 0: Not a Combination Product 02/01/2024 12/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 02/01/2024 12/31/2024 Labeler - Shantou Youjia E-Commerce Co., Ltd. (711173127) Establishment Name Address ID/FEI Business Operations Shantou Youjia E-Commerce Co., Ltd. 711173127 label(84067-949)
