Anticavity
NDC 37808-435, Sodium fluoride, mouthwash, from H E B.
- Product NDC
- 37808-435
- Status
- Listed
- Labeler
- H E B
- Dosage form
- MOUTHWASH
- 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/37808-435 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.1 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 37808-435-45 | 37808043545 | 946 mL in 1 BOTTLE, PLASTIC (37808-435-45) |
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 37808-435 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/37808-435 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 37808-435. 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.