FUZYAT 5% Minoxidil Hair Growth Treatment
- Product NDC
- 87408-035
- 11-digit product format
- 874080035
- Labeler code
- 87408
- Product ID
- 87408-035_5cdc3015-072d-af46-e063-6294a90ae66b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- 5% Minoxidil Hair Growth Treatment
- Dosage form
- SOLUTION/ DROPS
- Route
- TOPICAL
- Labeler
- Guangzhou Jingliang Cosmetics Co., Ltd.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-01
- 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
- FUZYAT 5% Minoxidil Hair Growth Treatment
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 5 g/100mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87408-035-01 | 87408003501 | 2 BOTTLE in 1 CARTON (87408-035-01) / 60 mL in 1 BOTTLE | 2 bottle | 2026-10-01 | No | No | Current |