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NDC 77782-012, SODIUM FLUORIDE, gel, dentifrice, from MKJ BRANDS LLC.
- Product NDC
- 77782-012
- Status
- Listed
- Labeler
- MKJ BRANDS LLC
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M021
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/77782-012 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.24 g/1000g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 77782-012-20 | 77782001220 | 1 BOTTLE in 1 BOX (77782-012-20) / 113 g in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 77782-012 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/77782-012 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 77782-012. 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.