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Sodium Fluoride 1.1% Gel

NDC 69367-310, Sodium Fluoride, gel, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-310
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/69367-310 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5 mg/g
Package NDCNDC-11Package
69367-310-56693670310561 TUBE in 1 CARTON (69367-310-56) / 56 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1822c957-0bd6-4e86-a030-80e6e428063a

  • NADAC price for package 69367031056

    GET /v1/drugs/nadac/69367031056

Use it

Look up 69367-310 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-310 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-310. 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.