Label: GZE MINOXIDIL SOLUTION- minoxidil liquid
- NDC Code(s): 83566-270-01
- Packager: Guangzhou Yilong Cosmetics Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 26, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PURPOSE
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- DO NOT USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
GZE MINOXIDIL SOLUTION
minoxidil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83566-270 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL 1-(2-METHYLBUTYRATE) (UNII: 9Q5W5G6461) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83566-270-01 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/26/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 06/26/2024 Labeler - Guangzhou Yilong Cosmetics Co., Ltd (712647107) Establishment Name Address ID/FEI Business Operations Guangzhou Yilong Cosmetics Co., Ltd 712647107 manufacture(83566-270)