Minoxidil
- Product NDC
- 70550-605
- 11-digit product format
- 705500605
- Labeler code
- 70550
- Product ID
- 70550-605_24fea157-1a8d-4e35-8575-104eecb09af1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- PROFECTUS BEAUTY LLC
- Application
- ANDA209074
- Marketing category
- ANDA
- Marketing start
- 2022-01-18
- Substance
- MINOXIDIL
- Active strength
- 50 mg/g
- 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
- Minoxidil
- Brand name suffix
- 5 Percent (For Women)
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 50 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 645146 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70550-605-04 | Minoxidil 5 Percent (For Women) | 60 g in 1 CAN | AEROSOL, FOAM | 60 | | 1 |
| 70550-605-04 | Minoxidil 5 Percent (For Women) | 1 in 1 CARTON | AEROSOL, FOAM | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70550-605 | MINOXIDIL 5 PERCENT (FOR WOMEN) (MINOXIDIL) AEROSOL, FOAM [PROFECTUS BEAUTY LLC] | 1 | Current NDC, Legacy NDC, 2 package rows | 20220120_b307bcb7-4659-4dd7-86aa-00b3735f5844.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70550-605-04 | 70550060504 | 1 CAN in 1 CARTON (70550-605-04) / 60 g in 1 CAN | 1 can | 2022-01-18 | 0000-00-00 | No | No | Current |