Keeps Minoxidil Topical Solution, 5%
- Product NDC
- 71713-102
- 11-digit product format
- 717130102
- Labeler code
- 71713
- Product ID
- 71713-102_3bce6383-1106-5096-e063-6294a90ae8ff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil Solution
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Keeps (30 Madison)
- Application
- ANDA217998
- Marketing category
- ANDA
- Marketing start
- 2025-08-31
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Keeps Minoxidil Topical Solution, 5%
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 311724 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71713-102-04 | Keeps Minoxidil Topical Solution, 5% | 60 mL in 1 BOTTLE | SOLUTION | 60 | | 2 |
| 71713-102-09 | Keeps Minoxidil Topical Solution, 5% | 3 in 1 CARTON | SOLUTION | 3 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71713-102-04 | 71713010204 | 60 mL in 1 BOTTLE | 60 ml | | | | Historical |
| 71713-102-09 | 71713010209 | 3 BOTTLE in 1 CARTON (71713-102-09) / 60 mL in 1 BOTTLE (71713-102-04) | 3 bottle | 2025-08-31 | No | No | Historical |