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Mucus Relief

Active substance: ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE HEPATICA VAR. OBTUSA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, LOBARIA PULMONARIA

TABLET · ANTIMONY POTASSIUM TARTRATE 5 [hp_X]/1, ATROPA BELLADONNA 6 [hp_X]/1, BRYONIA ALBA WHOLE 6 [hp_X]/1, ANEMONE HEPATICA VAR. OBTUSA 6 [hp_X]/1, HYOSCYAMUS NIGER 5 [hp_X]/1, IPECAC 6 [hp_X]/1, LOBELIA INFLATA 4 [hp_X]/1, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_X]/1, LOBARIA PULMONARIA 5 [hp_X]/1

United StatesActive

Marketing holder: MediNatura Inc

Verified 2026-10-09 · openFDA NDC

Composition
  • ANTIMONY POTASSIUM TARTRATE · 5 [hp_X]/1
  • ATROPA BELLADONNA · 6 [hp_X]/1
  • BRYONIA ALBA WHOLE · 6 [hp_X]/1
  • ANEMONE HEPATICA VAR. OBTUSA · 6 [hp_X]/1
  • HYOSCYAMUS NIGER · 5 [hp_X]/1
  • IPECAC · 6 [hp_X]/1
  • LOBELIA INFLATA · 4 [hp_X]/1
  • HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED · 30 [hp_X]/1
  • LOBARIA PULMONARIA · 5 [hp_X]/1
Registration
Registration number
62795-1012
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 62795-1012 · Verified 2026-10-09 · open in source