Minoxidil Topical Solution
- Product NDC
- 87399-001
- 11-digit product format
- 873990001
- Labeler code
- 87399
- Product ID
- 87399-001_4cd1163f-76c0-8700-e063-6294a90a3688
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil Topical Solution
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Growth Essence LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-13
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Minoxidil Topical Solution
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 2 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87399-001-01 | 87399000101 | 500 mL in 1 BOTTLE (87399-001-01) | 500 ml | 2026-03-13 | No | No | Historical |