Label: LIQUID spray
- NDC Code(s): 84067-442-01
- Packager: Shantou Youjia E-Commerce Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated May 24, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LIQUID
liquid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84067-442 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARGININE (UNII: 94ZLA3W45F) (ARGININE - UNII:94ZLA3W45F) ARGININE 7.5 mg in 50 mL HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID 10.5 mg in 50 mL ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 12.5 mg in 50 mL Inactive Ingredients Ingredient Name Strength GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000) (UNII: 0K9R94573C) 4.5 mg in 50 mL ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL) 7.5 mg in 50 mL PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) 7.5 mg in 50 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84067-442-01 50 mL 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(84067-442)
