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Flotrex

Active substance: SODIUM FLUORIDE, VITAMIN A, ASCORBIC ACID, SODIUM ASCORBATE, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN

TABLET, CHEWABLE · SODIUM FLUORIDE 1 mg/1, VITAMIN A 750 ug/1, ASCORBIC ACID 24 mg/1, SODIUM ASCORBATE 36 mg/1, CHOLECALCIFEROL 10 ug/1, .ALPHA.-TOCOPHEROL ACETATE, DL- 6.75 mg/1, THIAMINE MONONITRATE 1.05 mg/1, RIBOFLAVIN 1.2 mg/1, NIACINAMIDE 13.5 mg/1, PYRIDOXINE HYDROCHLORIDE 1.05 mg/1, FOLIC ACID 300 ug/1, CYANOCOBALAMIN 4.5 ug/1

United StatesActive

Marketing holder: PureTek Corporation

Verified 2026-10-09 · openFDA NDC

Composition
Registration
Registration number
59088-020
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 59088-020 · Verified 2026-10-09 · open in source