Minoxidil Serum
- Product NDC
- 87593-104
- 11-digit product format
- 875930104
- Labeler code
- 87593
- Product ID
- 87593-104_5d507b2e-92d0-647b-e063-6294a90a6cf3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil Serum
- Dosage form
- LIQUID
- Route
- CUTANEOUS
- Labeler
- Lance (Guangzhou) Biological Technology Co., Ltd.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-03-20
- Substance
- MINOXIDIL
- Active strength
- 2.5 g/50g
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- 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
- Minoxidil Serum
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 2.5 g/50g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87593-104-50 | 87593010450 | 50 g in 1 BOX (87593-104-50) | 50 g | 2025-03-20 | No | No | Current |