KOLORZ NEUTRAL FLUORIDE FOAM TRIPLE MINT
NDC 25047-765, SODIUM FLUORIDE, aerosol, foam, from DMG AMERICA, LLC.
- Product NDC
- 25047-765
- Status
- Listed
- Labeler
- DMG AMERICA, LLC
- Dosage form
- AEROSOL, FOAM
- Route
- DENTAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/25047-765 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.9 mg/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 25047-765-44 | 25047076544 | 125 g in 1 CAN (25047-765-44) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b83c62be-8e9d-4fa2-aa10-d34c88bf2387
Use it
Look up 25047-765 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/25047-765 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 25047-765. 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.