Alpha-Pro
NDC 55346-0942, Sodium Fluoride and Hydrofluoric Acid, gel, from Dental Technologies, Inc..
- Product NDC
- 55346-0942
- Status
- Listed
- Labeler
- Dental Technologies, Inc.
- Dosage form
- GEL
- Route
- DENTAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/55346-0942 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE7.9 mg/g
- HYDROFLUORIC ACID4.4 mg/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 55346-0942-1 | 55346094201 | 497 g in 1 BOTTLE (55346-0942-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/efe3646d-9eb1-4a49-aeb4-c4c224056851
Use it
Look up 55346-0942 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/55346-0942 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 55346-0942. 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.