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Sodium Fluoride 5000 Plus

NDC 69367-309, Sodium Fluoride, cream, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-309
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
CREAM
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/69367-309 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5 mg/g
Package NDCNDC-11Package
69367-309-51693670309511 TUBE in 1 CARTON (69367-309-51) / 51 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/157b975e-0229-4081-8d7d-b5f933e178e0
  • NADAC price for package 69367030951

    GET /v1/drugs/nadac/69367030951

Use it

Look up 69367-309 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-309 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-309. 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.