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Oxaltem

Active substance: BERBERIS VULGARIS ROOT BARK, OXALIC ACID DIHYDRATE, SANGUINARIA CANADENSIS ROOT, CHIMAPHILA UMBELLATA WHOLE, CALCIUM FLUORIDE, CALCIUM SILICATE, URIC ACID, TRIBASIC CALCIUM PHOSPHATE, PARATHYROID HORMONE, PYRIDOXINE HYDROCHLORIDE

LIQUID · BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL, OXALIC ACID DIHYDRATE 6 [hp_X]/mL, SANGUINARIA CANADENSIS ROOT 9 [hp_X]/mL, CHIMAPHILA UMBELLATA WHOLE 9 [hp_X]/mL, CALCIUM FLUORIDE 12 [hp_X]/mL, CALCIUM SILICATE 12 [hp_X]/mL, URIC ACID 12 [hp_X]/mL, TRIBASIC CALCIUM PHOSPHATE 6 [hp_C]/mL, PARATHYROID HORMONE 9 [hp_C]/mL, PYRIDOXINE HYDROCHLORIDE 12 [hp_C]/mL

United StatesActive

Marketing holder: Nucleic Products, LLC

Verified 2026-10-09 · openFDA NDC

Composition
Registration
Registration number
75053-0012
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 75053-0012 · Verified 2026-10-09 · open in source