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Dizziness HP

Active substance: OYSTER SHELL CALCIUM CARBONATE, CRUDE, DYSPHANIA AMBROSIOIDES, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, SILICON DIOXIDE, TOBACCO LEAF

LIQUID · OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL, DYSPHANIA AMBROSIOIDES 30 [hp_X]/mL, ANAMIRTA COCCULUS SEED 30 [hp_X]/mL, CONIUM MACULATUM FLOWERING TOP 30 [hp_X]/mL, STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/mL, PHOSPHORUS 30 [hp_X]/mL, PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL, SILICON DIOXIDE 30 [hp_X]/mL, TOBACCO LEAF 30 [hp_X]/mL

United StatesActive

Marketing holder: Energique, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 30 [hp_X]/mL
  • DYSPHANIA AMBROSIOIDES · 30 [hp_X]/mL
  • ANAMIRTA COCCULUS SEED · 30 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP · 30 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED · 30 [hp_X]/mL
  • PHOSPHORUS · 30 [hp_X]/mL
  • PULSATILLA PRATENSIS WHOLE · 30 [hp_X]/mL
  • SILICON DIOXIDE · 30 [hp_X]/mL
  • TOBACCO LEAF · 30 [hp_X]/mL
Registration
Registration number
44911-0187
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 44911-0187 · Verified 2026-10-09 · open in source