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BM BM115 DROPS

Active substance: POTASSIUM PERMANGANATE, RUEHSSIA CUNDURANGO BARK, NITRIC ACID, GOLDENSEAL, SODIUM BORATE, MERCURIUS SOLUBILIS, SULFURIC ACID, CAPSICUM

LIQUID · POTASSIUM PERMANGANATE 3 [hp_X]/mL, RUEHSSIA CUNDURANGO BARK 6 [hp_X]/mL, NITRIC ACID 100 [hp_X]/mL, GOLDENSEAL 3 [hp_X]/mL, SODIUM BORATE 100 [hp_X]/mL, MERCURIUS SOLUBILIS 100 [hp_X]/mL, SULFURIC ACID 100 [hp_X]/mL, CAPSICUM 100 [hp_X]/mL

United StatesActive

Marketing holder: BM Private Limited

Verified 2026-10-09 · openFDA NDC

Composition
  • POTASSIUM PERMANGANATE · 3 [hp_X]/mL
  • RUEHSSIA CUNDURANGO BARK · 6 [hp_X]/mL
  • NITRIC ACID · 100 [hp_X]/mL
  • GOLDENSEAL · 3 [hp_X]/mL
  • SODIUM BORATE · 100 [hp_X]/mL
  • MERCURIUS SOLUBILIS · 100 [hp_X]/mL
  • SULFURIC ACID · 100 [hp_X]/mL
  • CAPSICUM · 100 [hp_X]/mL
Registration
Registration number
85816-2115
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 85816-2115 · Verified 2026-10-09 · open in source