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Cough Relief Syrup

Active substance: ALTHAEA OFFICINALIS ROOT, ANTIMONY PENTASULFIDE, ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, CETRARIA ISLANDICA SUBSP. ISLANDICA, MATRICARIA RECUTITA, DROSERA ROTUNDIFOLIA, ECHINACEA ANGUSTIFOLIA, IPECAC, POTASSIUM CHLORIDE, PLANTAGO LANCEOLATA POLLEN, RUMEX CRISPUS ROOT, POLYGALA SENEGA ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, SUS SCROFA THYMUS, TRIFOLIUM PRATENSE FLOWER, URTICA DIOICA, VERBASCUM THAPSUS

LIQUID · ALTHAEA OFFICINALIS ROOT 1 [hp_X]/148mL, ANTIMONY PENTASULFIDE 12 [hp_X]/148mL, ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/148mL, BRYONIA ALBA ROOT 6 [hp_X]/148mL, CETRARIA ISLANDICA SUBSP. ISLANDICA 1 [hp_X]/148mL, MATRICARIA RECUTITA 1 [hp_X]/148mL, DROSERA ROTUNDIFOLIA 6 [hp_X]/148mL, ECHINACEA ANGUSTIFOLIA 1 [hp_X]/148mL, IPECAC 6 [hp_X]/148mL, POTASSIUM CHLORIDE 6 [hp_X]/148mL, PLANTAGO LANCEOLATA POLLEN 1 [hp_X]/148mL, RUMEX CRISPUS ROOT 6 [hp_X]/148mL, POLYGALA SENEGA ROOT 6 [hp_X]/148mL, SPONGIA OFFICINALIS SKELETON, ROASTED 6 [hp_X]/148mL, SUS SCROFA THYMUS 1 [hp_X]/148mL, TRIFOLIUM PRATENSE FLOWER 1 [hp_X]/148mL, URTICA DIOICA 1 [hp_X]/148mL, VERBASCUM THAPSUS 1 [hp_X]/148mL

United StatesActive

Marketing holder: OHM PHARMA INC.

Verified 2026-10-09 · openFDA NDC

Composition
  • ALTHAEA OFFICINALIS ROOT · 1 [hp_X]/148mL
  • ANTIMONY PENTASULFIDE · 12 [hp_X]/148mL
  • ANTIMONY POTASSIUM TARTRATE · 6 [hp_X]/148mL
  • BRYONIA ALBA ROOT · 6 [hp_X]/148mL
  • CETRARIA ISLANDICA SUBSP. ISLANDICA · 1 [hp_X]/148mL
  • MATRICARIA RECUTITA · 1 [hp_X]/148mL
  • DROSERA ROTUNDIFOLIA · 6 [hp_X]/148mL
  • ECHINACEA ANGUSTIFOLIA · 1 [hp_X]/148mL
  • IPECAC · 6 [hp_X]/148mL
  • POTASSIUM CHLORIDE · 6 [hp_X]/148mL
  • PLANTAGO LANCEOLATA POLLEN · 1 [hp_X]/148mL
  • RUMEX CRISPUS ROOT · 6 [hp_X]/148mL
  • POLYGALA SENEGA ROOT · 6 [hp_X]/148mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED · 6 [hp_X]/148mL
  • SUS SCROFA THYMUS · 1 [hp_X]/148mL
  • TRIFOLIUM PRATENSE FLOWER · 1 [hp_X]/148mL
  • URTICA DIOICA · 1 [hp_X]/148mL
  • VERBASCUM THAPSUS · 1 [hp_X]/148mL
Registration
Registration number
66096-709
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.13 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.14 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.15 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.16 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source
  • ingredients.17 · openFDA NDC · 66096-709 · Verified 2026-10-09 · open in source