Ice Pop Flavor Sodium Fluoride Anticavity Toothpast
NDC 83013-328, Sodium Fluoride, gel, from HISMILE PTY LTD.
- Product NDC
- 83013-328
- Status
- Listed
- Labeler
- HISMILE PTY LTD
- Dosage form
- GEL
- 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/83013-328 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.243 g/100g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 83013-328-06 | 83013032806 | 60 g in 1 BOTTLE, PUMP (83013-328-06) |
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 83013-328 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/83013-328 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 83013-328. 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.