UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE
Active substance: POTASSIUM NITRATE, SODIUM FLUORIDE
PASTE · POTASSIUM NITRATE 5 g/100g, SODIUM FLUORIDE .15 g/100g
United StatesActive
Marketing holder: Universal Distribution Center LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- POTASSIUM NITRATE · 5 g/100g
- SODIUM FLUORIDE · .15 g/100g
Registration
- Registration number
- 52000-109
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- DENTAL
Sources
- product · openFDA NDC · 52000-109 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 52000-109 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 52000-109 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 52000-109 · Verified 2026-10-09 · open in source