Sodium Fluoride and Potassium Nitrate
NDC 69367-318, Sodium Fluoride and Potassium Nitrate, gel, from Westminster Pharmaceuticals, LLC.
- Product NDC
- 69367-318
- Status
- Listed
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- GEL
- Route
- DENTAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69367-318 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE5.8 mg/mL
- POTASSIUM NITRATE57.5 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69367-318-01 | 69367031801 | 1 TUBE in 1 CARTON (69367-318-01) / 100 mL in 1 TUBE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/7a051d80-879d-4995-96ef-77b60dad26b7NADAC price for package 69367031801
GET /v1/drugs/nadac/69367031801
Use it
Look up 69367-318 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69367-318 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69367-318. 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.