Eczema Relief
Active substance: ARSENIC TRIIODIDE, POTASSIUM BROMIDE, POTASSIUM CHLORIDE, SODIUM BROMIDE, NICKEL SULFATE HEXAHYDRATE, SULFUR IODIDE, VIOLA TRICOLOR, ZINC BROMIDE
LIQUID · ARSENIC TRIIODIDE 8 [hp_X]/59mL, POTASSIUM BROMIDE 4 [hp_X]/59mL, POTASSIUM CHLORIDE 4 [hp_X]/59mL, SODIUM BROMIDE 4 [hp_X]/59mL, NICKEL SULFATE HEXAHYDRATE 5 [hp_X]/59mL, SULFUR IODIDE 14 [hp_X]/59mL, VIOLA TRICOLOR 12 [hp_X]/59mL, ZINC BROMIDE 6 [hp_X]/59mL
United StatesActive
Marketing holder: OHM PHARMA INC.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- ARSENIC TRIIODIDE · 8 [hp_X]/59mL
- POTASSIUM BROMIDE · 4 [hp_X]/59mL
- POTASSIUM CHLORIDE · 4 [hp_X]/59mL
- SODIUM BROMIDE · 4 [hp_X]/59mL
- NICKEL SULFATE HEXAHYDRATE · 5 [hp_X]/59mL
- SULFUR IODIDE · 14 [hp_X]/59mL
- VIOLA TRICOLOR · 12 [hp_X]/59mL
- ZINC BROMIDE · 6 [hp_X]/59mL
Registration
- Registration number
- 66096-192
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 66096-192 · Verified 2026-10-09 · open in source