MINOXIDIL 5% (FOR MEN)
NDC 21130-208, MINOXIDIL, aerosol, foam, from Better Living Brands, LLC.
- Product NDC
- 21130-208
- Status
- Listed
- Labeler
- Better Living Brands, LLC
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA218616
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/21130-208 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MINOXIDIL50 mg/g
Pharmacologic classes
Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 21130-208-03 | 21130020803 | 3 CAN in 1 CARTON (21130-208-03) / 60 g in 1 CAN |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 21130-208 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/21130-208 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 21130-208. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.