UREA
NDC 81542-201, UREA, lotion, from Bantry Pharma, LLC.
- Product NDC
- 81542-201
- Status
- Listed
- Labeler
- Bantry Pharma, LLC
- Dosage form
- LOTION
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/81542-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- UREA400 mg/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 81542-201-08 | 81542020108 | 226.8 g in 1 BOTTLE (81542-201-08) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cb6ddbfc-ea6a-0ddc-e053-2995a90aedc4
Use it
Look up 81542-201 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/81542-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 81542-201. 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.