Label: BOTOX FACIAL SERUM liquid
- NDC Code(s): 84025-239-01
- Packager: Guangzhou Yanxi Biotechnology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 28, 2024
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- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
BOTOX FACIAL SERUM
botox facial serum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84025-239 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) (BUTYLENE GLYCOL - UNII:3XUS85K0RA) BUTYLENE GLYCOL 3 mg in 100 mL BIOTINOYL TRIPEPTIDE-1 (UNII: O6380721VA) (BIOTINOYL TRIPEPTIDE-1 - UNII:O6380721VA) BIOTINOYL TRIPEPTIDE-1 5 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84025-239-01 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/28/2024 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 10/28/2024 Labeler - Guangzhou Yanxi Biotechnology Co., Ltd (632583102) Establishment Name Address ID/FEI Business Operations Guangzhou Yanxi Biotechnology Co., Ltd 632583102 manufacture(84025-239)
