5% Minoxidil for Men and Women
- Product NDC
- 84025-332
- 11-digit product format
- 840250332
- Labeler code
- 84025
- Product ID
- 84025-332_5be2bcec-0eb6-0741-e063-6294a90a83c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- 5% Minoxidil for Men and Women
- Dosage form
- SPRAY
- Route
- CUTANEOUS
- Labeler
- Guangzhou Yanxi Biotechnology Co., Ltd
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-20
- Substance
- BIOTIN; TOCOPHEROL
- Active strength
- .05; .05 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 5% Minoxidil for Men and Women
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BIOTIN | .05 g/100g |
| TOCOPHEROL | .05 g/100g |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 84025-332-01 | 84025033201 | 80 g in 1 BOTTLE (84025-332-01) | 80 g | 2026-09-20 | No | No | Current |