Opalescence Whitening Sensitivity Relief
Active substance: SODIUM FLUORIDE, POTASSIUM NITRATE
GEL, DENTIFRICE · SODIUM FLUORIDE 1.1 mg/g, POTASSIUM NITRATE 50 mg/g
United StatesActive
Marketing holder: Ultradent Products, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- SODIUM FLUORIDE · 1.1 mg/g
- POTASSIUM NITRATE · 50 mg/g
Registration
- Registration number
- 51206-315
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- DENTAL
Sources
- product · openFDA NDC · 51206-315 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 51206-315 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 51206-315 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 51206-315 · Verified 2026-10-09 · open in source