Sodium Fluoride 5000 ppm Sensitive
NDC 11527-704, Sodium Fluoride1.1%, Potassium Nitrate 5%, gel, dentifrice, from Sheffield Pharmaceuticals LLC.
- Product NDC
- 11527-704
- Status
- Listed
- Labeler
- Sheffield Pharmaceuticals 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/11527-704 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE5.8 mg/mL
- POTASSIUM NITRATE57.5 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 11527-704-42 | 11527070442 | 1 TUBE in 1 CARTON (11527-704-42) / 100 mL in 1 TUBE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/02f4cf0b-188c-4522-b759-ffe4a9d150e8NADAC price for package 11527070442
GET /v1/drugs/nadac/11527070442
Use it
Look up 11527-704 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/11527-704 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 11527-704. 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.