AllergiClear-M
Active substance: CALCIUM PHOSPHATE, CALCIUM FLUORIDE, EUPHRASIA OFFICINALIS LEAF, EPINEPHRINE, HISTAMINE DIHYDROCHLORIDE, SILICON DIOXIDE, SODIUM CHLORIDE, POTASSIUM CHLORIDE
LIQUID · CALCIUM PHOSPHATE 8 [hp_X]/59mL, CALCIUM FLUORIDE 8 [hp_X]/59mL, EUPHRASIA OFFICINALIS LEAF 4 [hp_X]/59mL, EPINEPHRINE 7 [hp_C]/59mL, HISTAMINE DIHYDROCHLORIDE 7 [hp_C]/59mL, SILICON DIOXIDE 8 [hp_X]/59mL, SODIUM CHLORIDE 8 [hp_X]/59mL, POTASSIUM CHLORIDE 8 [hp_X]/59mL
United StatesActive
Marketing holder: Silver Star Brands
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- CALCIUM PHOSPHATE · 8 [hp_X]/59mL
- CALCIUM FLUORIDE · 8 [hp_X]/59mL
- EUPHRASIA OFFICINALIS LEAF · 4 [hp_X]/59mL
- EPINEPHRINE · 7 [hp_C]/59mL
- HISTAMINE DIHYDROCHLORIDE · 7 [hp_C]/59mL
- SILICON DIOXIDE · 8 [hp_X]/59mL
- SODIUM CHLORIDE · 8 [hp_X]/59mL
- POTASSIUM CHLORIDE · 8 [hp_X]/59mL
Registration
- Registration number
- 68703-341
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 68703-341 · Verified 2026-10-09 · open in source