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Sodium Fluoride and Potassium Nitrate

NDC 69367-318, Sodium Fluoride and Potassium Nitrate, gel, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-318
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
GEL
Route
DENTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-318 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5.8 mg/mL
  • POTASSIUM NITRATE57.5 mg/mL
Package NDCNDC-11Package
69367-318-01693670318011 TUBE in 1 CARTON (69367-318-01) / 100 mL in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7a051d80-879d-4995-96ef-77b60dad26b7
  • NADAC price for package 69367031801

    GET /v1/drugs/nadac/69367031801

Use it

Look up 69367-318 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-318 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-318. 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.