Label: 2% WOMEN MINOXIDIL HAIR STRENGTHENING SET- minoxidil liquid
- NDC Code(s): 83566-555-01
- Packager: Guangdong Aimu Biological Technology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 30, 2024
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- Active ingredients
- Purpose
- Uses
- Warnings
- Stop use and ask a doctor if
- Do not use
- When using this product
- Keep out of reach of children.
- Dosage
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
2% WOMEN MINOXIDIL HAIR STRENGTHENING SET
minoxidil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83566-555 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 2 g in 100 mL Inactive Ingredients Ingredient Name Strength ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALCOHOL (UNII: 3K9958V90M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ) DIPROPYLENE GLYCOL (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83566-555-01 60 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package 07/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 07/31/2024 Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107) Establishment Name Address ID/FEI Business Operations Guangdong Aimu Biological Technology Co., Ltd 712647107 manufacture(83566-555)