Sodium Fluoride and Potassium Nitrate
Active substance: SODIUM FLUORIDE, POTASSIUM NITRATE
GEL · SODIUM FLUORIDE 5.8 mg/mL, POTASSIUM NITRATE 57.5 mg/mL
United StatesActive
Marketing holder: Westminster Pharmaceuticals, LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- SODIUM FLUORIDE · 5.8 mg/mL
- POTASSIUM NITRATE · 57.5 mg/mL
Registration
- Registration number
- 69367-318
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- DENTAL
Sources
- product · openFDA NDC · 69367-318 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 69367-318 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 69367-318 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 69367-318 · Verified 2026-10-09 · open in source