Allergy

Active substance: ONION, AMBROSIA ARTEMISIIFOLIA WHOLE, ACTIVATED CHARCOAL, EUPHRASIA STRICTA, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA VULGARIS WHOLE, SULFUR, SOLIDAGO VIRGAUREA FLOWERING TOP

LIQUID · ONION 30 [hp_C]/mL, AMBROSIA ARTEMISIIFOLIA WHOLE 30 [hp_C]/mL, ACTIVATED CHARCOAL 30 [hp_C]/mL, EUPHRASIA STRICTA 30 [hp_C]/mL, STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/mL, PHOSPHORUS 30 [hp_C]/mL, PULSATILLA VULGARIS WHOLE 30 [hp_C]/mL, SULFUR 30 [hp_C]/mL, SOLIDAGO VIRGAUREA FLOWERING TOP 30 [hp_C]/mL

United StatesActive

Marketing holder: Zorex International

Verified 2026-10-09 · openFDA NDC

Source: openFDA NDC
Countries with the substance registered: 1

Composition

ONION · 30 [hp_C]/mL
AMBROSIA ARTEMISIIFOLIA WHOLE · 30 [hp_C]/mL
ACTIVATED CHARCOAL · 30 [hp_C]/mL
EUPHRASIA STRICTA · 30 [hp_C]/mL
STRYCHNOS NUX-VOMICA SEED · 30 [hp_C]/mL
PHOSPHORUS · 30 [hp_C]/mL
PULSATILLA VULGARIS WHOLE · 30 [hp_C]/mL
SULFUR · 30 [hp_C]/mL
SOLIDAGO VIRGAUREA FLOWERING TOP · 30 [hp_C]/mL

Registration

Registration number: 81825-0007
Registration status: Active
Dispensing: Over the counter
Route: ORAL

Sources

product · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 81825-0007 · Verified 2026-10-09 · open in source