Ionite APF
NDC 53045-206, Sodium Fluoride, gel, from Dharma Research, inc..
- Product NDC
- 53045-206
- Status
- Listed
- Labeler
- Dharma Research, inc.
- Dosage form
- GEL
- Route
- DENTAL, ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/53045-206 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE6.027 g/490g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 53045-206-08 | 53045020608 | 245 g in 1 BOTTLE (53045-206-08) |
| 53045-206-17 | 53045020617 | 490 g in 1 BOTTLE (53045-206-17) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/bc9664df-c4eb-4d29-b1c0-4d4dff6a75e4
Use it
Look up 53045-206 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/53045-206 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 53045-206. 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.