Label: GZE 5% MINOXIDIL SOLUTION- minoxidil 5% spray
- NDC Code(s): 74458-270-01
- Packager: Guangzhou Yilong Cosmetics Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 10, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- PURPOSE
- WARNINGS
- STOP USE
- DO NOT USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
GZE 5% MINOXIDIL SOLUTION
minoxidil 5% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74458-270 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 WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74458-270-01 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/19/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 09/19/2024 Labeler - Guangzhou Yilong Cosmetics Co., Ltd (420929116) Establishment Name Address ID/FEI Business Operations Guangzhou Yilong Cosmetics Co., Ltd 420929116 manufacture(74458-270)