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Cold

Active substance: ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, FERROSOFERRIC PHOSPHATE, GELSEMIUM SEMPERVIRENS ROOT, POTASSIUM DICHROMATE, POTASSIUM IODIDE, ZINC GLUCONATE

LIQUID · ACONITUM NAPELLUS 4 [hp_X]/59mL, BRYONIA ALBA ROOT 6 [hp_X]/59mL, EUPATORIUM PERFOLIATUM FLOWERING TOP 4 [hp_X]/59mL, FERROSOFERRIC PHOSPHATE 4 [hp_X]/59mL, GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/59mL, POTASSIUM DICHROMATE 6 [hp_X]/59mL, POTASSIUM IODIDE 6 [hp_X]/59mL, ZINC GLUCONATE 3 [hp_X]/59mL

United StatesActive

Marketing holder: OHM PHARMA INC.

Verified 2026-10-09 · openFDA NDC

Composition
  • ACONITUM NAPELLUS · 4 [hp_X]/59mL
  • BRYONIA ALBA ROOT · 6 [hp_X]/59mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP · 4 [hp_X]/59mL
  • FERROSOFERRIC PHOSPHATE · 4 [hp_X]/59mL
  • GELSEMIUM SEMPERVIRENS ROOT · 6 [hp_X]/59mL
  • POTASSIUM DICHROMATE · 6 [hp_X]/59mL
  • POTASSIUM IODIDE · 6 [hp_X]/59mL
  • ZINC GLUCONATE · 3 [hp_X]/59mL
Registration
Registration number
66096-114
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 66096-114 · Verified 2026-10-09 · open in source