PRO Gel 5000 Mint
NDC 61578-215, Sodium fluoride, gel, dentifrice, from DENTAL ALLIANCE HOLDINGS LLC.
- Product NDC
- 61578-215
- Status
- Listed
- Labeler
- DENTAL ALLIANCE HOLDINGS LLC
- 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/61578-215 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE5000 ug/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 61578-215-01 | 61578021501 | 68 g in 1 TUBE, WITH APPLICATOR (61578-215-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f127e236-5207-948b-e053-2a95a90ab740
Use it
Look up 61578-215 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/61578-215 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 61578-215. 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.