Foot Powder
NDC 0363-7999, Miconazole Nitrate, powder, from Walgreens Company.
- Product NDC
- 0363-7999
- Status
- Listed
- Labeler
- Walgreens Company
- Dosage form
- POWDER
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M005
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0363-7999 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MICONAZOLE NITRATE20 mg/g
Pharmacologic classes
Azole Antifungal [EPC]; Azoles [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0363-7999-01 | 00363799901 | 71 g in 1 BOTTLE, PLASTIC (0363-7999-01) |
| 0363-7999-03 | 00363799903 | 85 g in 1 BOTTLE, PLASTIC (0363-7999-03) |
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 0363-7999 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0363-7999 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0363-7999. 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.