hair treatment
- Product NDC
- 87022-009
- 11-digit product format
- 870220009
- Labeler code
- 87022
- Product ID
- 87022-009_3d84eb2d-f0a8-a21c-e063-6294a90aeef5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- LABORATORIO MK SRL
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-22
- Marketing end
- 2027-08-20
- Substance
- MINOXIDIL
- Active strength
- 1 mg/473mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- hair treatment
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 1 mg/473mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87022-009-25 | hair treatment | 473 mL in 1 JAR | CREAM | 473 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 87022-009-25 | 87022000925 | 473 mL in 1 JAR (87022-009-25) | 473 ml | 2025-08-22 | 2027-08-20 | Yes | No | Historical |