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Mentox HP

Active substance: GOLD, BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS

LIQUID · GOLD 30 [hp_X]/mL, BARIUM CARBONATE 30 [hp_X]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL, LACHESIS MUTA VENOM 30 [hp_X]/mL, LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL, SODIUM CHLORIDE 30 [hp_X]/mL, STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/mL, PHOSPHORUS 30 [hp_X]/mL

United StatesActive

Marketing holder: Energique, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • GOLD · 30 [hp_X]/mL
  • BARIUM CARBONATE · 30 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 30 [hp_X]/mL
  • LACHESIS MUTA VENOM · 30 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE · 30 [hp_X]/mL
  • SODIUM CHLORIDE · 30 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED · 30 [hp_X]/mL
  • PHOSPHORUS · 30 [hp_X]/mL
Registration
Registration number
44911-0299
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 44911-0299 · Verified 2026-10-09 · open in source