Pro-Den Rx
NDC 59883-720, Stannous Fluoride, rinse, from Den-mat Holdings, Llc.
- Product NDC
- 59883-720
- Status
- Listed
- Labeler
- Den-mat Holdings, 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/59883-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- STANNOUS FLUORIDE1.53 mg/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59883-720-08 | 59883072008 | 1 BOTTLE in 1 CARTON (59883-720-08) / 283.5 g in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 59883-720 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59883-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59883-720. 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.