Sodium Fluoride Gel
NDC 50268-733, Sodium Fluoride, gel, dentifrice, from AvPAK.
- Product NDC
- 50268-733
- Status
- Listed
- Labeler
- AvPAK
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50268-733 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE5 mg/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50268-733-56 | 50268073356 | 1 TUBE in 1 CARTON (50268-733-56) / 56 g in 1 TUBE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/de973f9c-af34-4977-e053-2995a90a54a0NADAC price for package 50268073356
GET /v1/drugs/nadac/50268073356
Use it
Look up 50268-733 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50268-733 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50268-733. 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.