BM BM38 DROPS
Active substance: BERBERIS AQUIFOLIUM ROOT BARK, SULFUR IODIDE, POTASSIUM IODIDE, GRAPHITE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, CENTELLA ASIATICA WHOLE, POTASSIUM BROMIDE
LIQUID · BERBERIS AQUIFOLIUM ROOT BARK 2 [hp_X]/mL, SULFUR IODIDE 7 [hp_X]/mL, POTASSIUM IODIDE 7 [hp_X]/mL, GRAPHITE 18 [hp_X]/mL, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/mL, CENTELLA ASIATICA WHOLE 2 [hp_X]/mL, POTASSIUM BROMIDE 7 [hp_X]/mL
United StatesActive
Marketing holder: BM Private Limited
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- BERBERIS AQUIFOLIUM ROOT BARK · 2 [hp_X]/mL
- SULFUR IODIDE · 7 [hp_X]/mL
- POTASSIUM IODIDE · 7 [hp_X]/mL
- GRAPHITE · 18 [hp_X]/mL
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE · 12 [hp_X]/mL
- CENTELLA ASIATICA WHOLE · 2 [hp_X]/mL
- POTASSIUM BROMIDE · 7 [hp_X]/mL
Registration
- Registration number
- 85816-2038
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 85816-2038 · Verified 2026-10-09 · open in source