United States · FDA National Drug Code directory
Sodium Fluoride and Potassium Nitrate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69367-318_0c9c8462-f962-4615-8649-dea8e1ecb498
- Product NDC
- 69367-318
- Form
- GEL
- Composition / generic term
- Sodium Fluoride and Potassium Nitrate
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20220615
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM FLUORIDE — 5.8 mg/mL
- POTASSIUM NITRATE — 57.5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (69367-318-01) / 100 mL in 1 TUBE · 69367-318-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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