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Earache Relief

Active substance: ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, MATRICARIA CHAMOMILLA WHOLE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LYCOPODIUM CLAVATUM SPORE, PLANTAGO MAJOR WHOLE, PULSATILLA VULGARIS WHOLE

TABLET · ATROPA BELLADONNA 12 [hp_X]/1, OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/1, MATRICARIA CHAMOMILLA WHOLE 12 [hp_X]/1, CALCIUM SULFIDE 12 [hp_X]/1, POTASSIUM DICHROMATE 12 [hp_X]/1, LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/1, PLANTAGO MAJOR WHOLE 12 [hp_X]/1, PULSATILLA VULGARIS WHOLE 12 [hp_X]/1

United StatesActive

Marketing holder: The Magni Company

Verified 2026-10-09 · openFDA NDC

Composition
  • ATROPA BELLADONNA · 12 [hp_X]/1
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 12 [hp_X]/1
  • MATRICARIA CHAMOMILLA WHOLE · 12 [hp_X]/1
  • CALCIUM SULFIDE · 12 [hp_X]/1
  • POTASSIUM DICHROMATE · 12 [hp_X]/1
  • LYCOPODIUM CLAVATUM SPORE · 12 [hp_X]/1
  • PLANTAGO MAJOR WHOLE · 12 [hp_X]/1
  • PULSATILLA VULGARIS WHOLE · 12 [hp_X]/1
Registration
Registration number
43689-0020
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 43689-0020 · Verified 2026-10-09 · open in source