Minoxidil Topical Solution
- Product NDC
- 87399-002
- 11-digit product format
- 873990002
- Labeler code
- 87399
- Product ID
- 87399-002_51e5e66c-9d83-4167-e063-6394a90a0891
- 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
- 2026-05-16
- 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
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 | 5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87399-002-01 | Minoxidil Topical Solution | 360 mL in 1 BOTTLE | LIQUID | 360 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87399-002-01 | 87399000201 | 360 mL in 1 BOTTLE (87399-002-01) | 360 ml | 2026-05-16 | No | No | Historical |