PRO-SYS
NDC 66975-778, Potassium Nitrate, Sodium Fluoride, paste, dentifrice, from Benco Dental.
- Product NDC
- 66975-778
- Status
- Listed
- Labeler
- Benco Dental
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL, ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/66975-778 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- POTASSIUM NITRATE5 g/100g
- SODIUM FLUORIDE1.1 g/100g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 66975-778-01 | 66975077801 | 113 g in 1 TUBE (66975-778-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4c9c144a-f28e-756d-e063-6394a90a5971
Use it
Look up 66975-778 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/66975-778 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 66975-778. 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.