ETERNAL MINOXIDIL
- Product NDC
- 79974-201
- 11-digit product format
- 799740201
- Labeler code
- 79974
- Product ID
- 79974-201_57f9a42b-bbc0-4cd2-bece-fb5bdcab2a02
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Miramar Cosmetic, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-03-17
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 79974-201-02 | 79974020102 | 1 BOTTLE, DROPPER in 1 BOX (79974-201-02) > 60 mL in 1 BOTTLE, DROPPER (79974-201-03) | 2022-03-17 | 0000-00-00 | No | No | Current |