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Sodium Fluoride 5000 PPM

NDC 69367-312, Sodium Fluoride, paste, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-312
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
PASTE
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/69367-312 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE6 mg/mL
Package NDCNDC-11Package
69367-312-0169367031201100 mL in 1 TUBE (69367-312-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56efb346-c715-463d-9260-f7fcfbd2b70f

  • NADAC price for package 69367031201

    GET /v1/drugs/nadac/69367031201

Use it

Look up 69367-312 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-312 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-312. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.