PureLife APF
NDC 68987-011, Sodium Fluoride, gel, from PureLife Dental.
- Product NDC
- 68987-011
- Status
- Listed
- Labeler
- PureLife Dental
- 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/68987-011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE5.6 g/454g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68987-011-15 | 68987001115 | 454 g in 1 BOTTLE, PLASTIC (68987-011-15) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6d3e9f0f-f5e9-44ec-9688-86276d33a8a8
Use it
Look up 68987-011 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68987-011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68987-011. 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.