AGIKENB 5% Minoxidil Hair Growth Foam
- Product NDC
- 85304-033
- Requested package NDC
- 85304-033-02
- 11-digit product format
- 853040033
- Labeler code
- 85304
- Product ID
- 85304-033_5c36588a-651d-435e-e063-6294a90a5a30
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Guangzhou Borderless Technology Co., Ltd.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-24
- Substance
- MINOXIDIL; BIOTIN
- Active strength
- .05; .005 g/mL; g/mL
- 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
- AGIKENB 5% Minoxidil Hair Growth Foam
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | .05 g/mL |
| BIOTIN | .005 g/mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85304-033-02 | 85304003302 | 8 BOTTLE in 1 PACKAGE (85304-033-02) / 60 mL in 1 BOTTLE | 8 bottle | 2026-09-24 | No | No | Current |