Pro-Den Rx
NDC 59883-911, Sodium Fluoride, rinse, from Den-Mat Holdings, Llc.
- Product NDC
- 59883-911
- Status
- Listed
- Labeler
- Den-Mat Holdings, Llc
- Dosage form
- RINSE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59883-911 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE9 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59883-911-64 | 59883091164 | 1890 mL in 1 BOTTLE, PLASTIC (59883-911-64) |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
FDA label sections
GET /v1/drugs/labels/ba020e07-ad41-4419-a503-f1245131b7d2
Use it
Look up 59883-911 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59883-911 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59883-911. 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.