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Allergy Relief Indoor and Outdoor

Active substance: ONION, AMBROSIA ARTEMISIIFOLIA WHOLE, ARSENIC TRIOXIDE, ARISAEMA TRIPHYLLUM ROOT, ARUNDO PLINIANA ROOT, EUPHRASIA STRICTA, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, POTASSIUM DICHROMATE, NAPHTHALENE, SODIUM CHLORIDE, SCHOENOCAULON OFFICINALE SEED, SOLIDAGO VIRGAUREA FLOWERING TOP, LOBARIA PULMONARIA, SULFUR, TRIFOLIUM PRATENSE FLOWER, WYETHIA HELENIOIDES ROOT

LIQUID · ONION 10 [hp_X]/59mL, AMBROSIA ARTEMISIIFOLIA WHOLE 10 [hp_X]/59mL, ARSENIC TRIOXIDE 10 [hp_X]/59mL, ARISAEMA TRIPHYLLUM ROOT 10 [hp_X]/59mL, ARUNDO PLINIANA ROOT 10 [hp_X]/59mL, EUPHRASIA STRICTA 10 [hp_X]/59mL, GALPHIMIA GLAUCA FLOWERING TOP 10 [hp_X]/59mL, HISTAMINE DIHYDROCHLORIDE 10 [hp_X]/59mL, POTASSIUM DICHROMATE 10 [hp_X]/59mL, NAPHTHALENE 10 [hp_X]/59mL, SODIUM CHLORIDE 10 [hp_X]/59mL, SCHOENOCAULON OFFICINALE SEED 10 [hp_X]/59mL, SOLIDAGO VIRGAUREA FLOWERING TOP 10 [hp_X]/59mL, LOBARIA PULMONARIA 10 [hp_X]/59mL, SULFUR 10 [hp_X]/59mL, TRIFOLIUM PRATENSE FLOWER 10 [hp_X]/59mL, WYETHIA HELENIOIDES ROOT 10 [hp_X]/59mL

United StatesActive

Marketing holder: King Bio Inc.

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
  • ONION · 10 [hp_X]/59mL
  • AMBROSIA ARTEMISIIFOLIA WHOLE · 10 [hp_X]/59mL
  • ARSENIC TRIOXIDE · 10 [hp_X]/59mL
  • ARISAEMA TRIPHYLLUM ROOT · 10 [hp_X]/59mL
  • ARUNDO PLINIANA ROOT · 10 [hp_X]/59mL
  • EUPHRASIA STRICTA · 10 [hp_X]/59mL
  • GALPHIMIA GLAUCA FLOWERING TOP · 10 [hp_X]/59mL
  • HISTAMINE DIHYDROCHLORIDE · 10 [hp_X]/59mL
  • POTASSIUM DICHROMATE · 10 [hp_X]/59mL
  • NAPHTHALENE · 10 [hp_X]/59mL
  • SODIUM CHLORIDE · 10 [hp_X]/59mL
  • SCHOENOCAULON OFFICINALE SEED · 10 [hp_X]/59mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP · 10 [hp_X]/59mL
  • LOBARIA PULMONARIA · 10 [hp_X]/59mL
  • SULFUR · 10 [hp_X]/59mL
  • TRIFOLIUM PRATENSE FLOWER · 10 [hp_X]/59mL
  • WYETHIA HELENIOIDES ROOT · 10 [hp_X]/59mL
Products containing arsenic trioxide in other countries

Showing products with this active substance, combinations included; the full composition is shown for each product.

CountryProducts
EU 4
Registration
Registration number
57955-9997
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.13 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.14 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.15 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source
  • ingredients.16 · openFDA NDC · 57955-9997 · Verified 2026-10-09 · open in source