Denta 5000 Plus
NDC 16571-814, Sodium fluoride, cream, from Rising Pharma Holdings, Inc..
- Product NDC
- 16571-814
- Status
- Listed
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- CREAM
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/16571-814 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE1.1 g/100g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 16571-814-50 | 16571081450 | 51 g in 1 TUBE (16571-814-50) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/7142eb93-54ff-4ba1-af43-3fa3dc1fad01NADAC price for package 16571081450
GET /v1/drugs/nadac/16571081450
Use it
Look up 16571-814 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/16571-814 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 16571-814. 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.