Inlifay Minoxidil TOPICAL
- Product NDC
- 87710-008
- Requested package NDC
- 87710-008-01
- 11-digit product format
- 877100008
- Labeler code
- 87710
- Product ID
- 87710-008_5d77bf1c-3fc6-6cc2-e063-6394a90a465d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Huanmei Cosmetics Co., Ltd.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-10
- Substance
- MINOXIDIL
- Active strength
- 5 g/100mL
- 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
- Inlifay Minoxidil TOPICAL
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MINOXIDIL | 5 g/100mL |
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 |
|---|---|---|---|---|---|---|---|
| 87710-008-01 | 87710000801 | 2 BOTTLE in 1 BOX (87710-008-01) / 60 mL in 1 BOTTLE | 2 bottle | 2026-10-10 | No | No | Current |