AUREVESSA 5% Minoxidil hair grow
- Product NDC
- 85163-027
- 11-digit product format
- 851630027
- Labeler code
- 85163
- Product ID
- 85163-027_5c381cf8-ba40-7762-e063-6394a90af4a5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GLYCERIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shantou Ouhoe Technology Co., Ltd.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-27
- Substance
- MINOXIDIL
- Active strength
- 3 mg/60mg
- 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
- AUREVESSA 5% Minoxidil hair grow
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MINOXIDIL | 3 mg/60mg |
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 |
|---|---|---|---|---|---|---|---|
| 85163-027-01 | 85163002701 | 60 mg in 1 BOX (85163-027-01) | 60 mg | 2026-09-27 | No | No | Current |