Acunol
Active substance: NICKEL SULFATE, POTASSIUM BROMIDE, SODIUM BROMIDE, ZINC SULFATE ANHYDROUS, SULFUR
TABLET · NICKEL SULFATE 1 [hp_X]/1, POTASSIUM BROMIDE 1 [hp_X]/1, SODIUM BROMIDE 1 [hp_X]/1, ZINC SULFATE ANHYDROUS 1 [hp_X]/1, SULFUR 1 [hp_X]/1
United StatesActive
Marketing holder: PLYMOUTH HEALTHCARE PRODUCTS LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- NICKEL SULFATE · 1 [hp_X]/1
- POTASSIUM BROMIDE · 1 [hp_X]/1
- SODIUM BROMIDE · 1 [hp_X]/1
- ZINC SULFATE ANHYDROUS · 1 [hp_X]/1
- SULFUR · 1 [hp_X]/1
Registration
- Registration number
- 61480-137
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 61480-137 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 61480-137 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 61480-137 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 61480-137 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 61480-137 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 61480-137 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 61480-137 · Verified 2026-10-09 · open in source