Label: LIQUID spray
- NDC Code(s): 84067-328-01
- Packager: Shantou Youjia E-Commerce Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated March 18, 2024
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INGREDIENTS AND APPEARANCE
LIQUID
liquid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84067-328 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 7.5 mg in 50 mg ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 10 mg in 50 mg PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 5 mg in 50 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 15 mL in 50 mg HYALURONATE SODIUM (UNII: YSE9PPT4TH) 12.5 mg in 50 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84067-328-01 50 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(84067-328)