GuruNanda Anti-Cavity
NDC 70708-890, Sodium Fluoride, rinse, from GURUNANDA, LLC.
- Product NDC
- 70708-890
- Status
- Listed
- Labeler
- GURUNANDA, LLC
- Dosage form
- RINSE
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M021
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70708-890 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.2 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70708-890-16 | 70708089016 | 473 mL in 1 BOTTLE (70708-890-16) |
| 70708-890-24 | 70708089024 | 710 mL in 1 BOTTLE (70708-890-24) |
| 70708-890-33 | 70708089033 | 999 mL in 1 BOTTLE (70708-890-33) |
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 70708-890 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70708-890 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70708-890. 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.