OHM Mucus Relief

Active substance: ANTIMONY TRISULFIDE, ANTIMONY POTASSIUM TARTRATE, CHELIDONIUM MAJUS, FERROSOFERRIC PHOSPHATE, POTASSIUM DICHROMATE, POTASSIUM CARBONATE, POTASSIUM CHLORIDE, POTASSIUM SULFATE, MARRUBIUM VULGARE

TABLET, CHEWABLE · ANTIMONY TRISULFIDE 6 [hp_C]/1, ANTIMONY POTASSIUM TARTRATE 6 [hp_C]/1, CHELIDONIUM MAJUS 6 [hp_X]/1, FERROSOFERRIC PHOSPHATE 6 [hp_X]/1, POTASSIUM DICHROMATE 12 [hp_X]/1, POTASSIUM CARBONATE 30 [hp_C]/1, POTASSIUM CHLORIDE 6 [hp_X]/1, POTASSIUM SULFATE 6 [hp_X]/1, MARRUBIUM VULGARE 9 [hp_C]/1

United StatesActive

Marketing holder: OHM PHARMA INC.

Verified 2026-10-09 · openFDA NDC

Source: openFDA NDC
Countries with the substance registered: 1

Composition

ANTIMONY TRISULFIDE · 6 [hp_C]/1
ANTIMONY POTASSIUM TARTRATE · 6 [hp_C]/1
CHELIDONIUM MAJUS · 6 [hp_X]/1
FERROSOFERRIC PHOSPHATE · 6 [hp_X]/1
POTASSIUM DICHROMATE · 12 [hp_X]/1
POTASSIUM CARBONATE · 30 [hp_C]/1
POTASSIUM CHLORIDE · 6 [hp_X]/1
POTASSIUM SULFATE · 6 [hp_X]/1
MARRUBIUM VULGARE · 9 [hp_C]/1

Registration

Registration number: 66096-706
Registration status: Active
Dispensing: Over the counter
Route: ORAL

Sources

product · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 66096-706 · Verified 2026-10-09 · open in source