Label: LIQUID liquid
- NDC Code(s): 84067-662-01
- Packager: Shantou Youjia E-Commerce Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated May 4, 2024
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INGREDIENTS AND APPEARANCE
LIQUID
liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84067-662 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL 1.5 mg in 15 mg GREEN TEA LEAF (UNII: W2ZU1RY8B0) (GREEN TEA LEAF - UNII:W2ZU1RY8B0) GREEN TEA LEAF 2.25 mg in 15 mg HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID 3 mg in 15 mg PEPTIDE-T (UNII: 05DYM3ZS1X) (PEPTIDE-T - UNII:05DYM3ZS1X) PEPTIDE-T 2.25 mg in 15 mg PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 1.5 mg in 15 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 4.5 mL in 15 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84067-662-01 15 mg in 1 BOX; 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(84067-662)
