PreviDent 5000 Sensitive
Active substance: SODIUM FLUORIDE, POTASSIUM NITRATE
GEL, DENTIFRICE · SODIUM FLUORIDE 5.8 mg/mL, POTASSIUM NITRATE 57.5 mg/mL
United StatesActive
Marketing holder: Colgate Oral Pharmaceuticals, Inc.
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
- 0126-0070
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- DENTAL
Sources
- product · openFDA NDC · 0126-0070 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 0126-0070 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 0126-0070 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 0126-0070 · Verified 2026-10-09 · open in source