PureLife APF
Active substance: sodium fluoride
GEL · SODIUM FLUORIDE 5.6 g/454g
United StatesActive
Marketing holder: PureLife Dental
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- SODIUM FLUORIDE · 5.6 g/454g
Registration
- Registration number
- 68987-011
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- DENTAL
Sources
- product · openFDA NDC · 68987-011 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 68987-011 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 68987-011 · Verified 2026-10-09 · open in source