MinoxidilTopical Serum
- Product NDC
- 87722-096
- 11-digit product format
- 877220096
- Labeler code
- 87722
- Product ID
- 87722-096_5c2b3706-aec6-bae3-e063-6394a90aa4fe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Guangdong Jiaoyu Biotechnology Co., Ltd
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-24
- Substance
- MINOXIDIL
- Active strength
- 5 mg/100mg
- 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
- MinoxidilTopical Serum
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MINOXIDIL | 5 mg/100mg |
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 |
|---|---|---|---|---|---|---|---|
| 87722-096-01 | 87722009601 | 200 mg in 1 BOTTLE (87722-096-01) | 200 mg | 2026-09-24 | No | No | Current |