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Lipostat

Active substance: CAPSICUM, FUCUS VESICULOSUS, BORAGE, EGG PHOSPHOLIPIDS, OYSTER SHELL CALCIUM CARBONATE, CRUDE, IRON, POTASSIUM DICHROMATE, POTASSIUM CARBONATE, PULSATILLA PRATENSIS WHOLE, SULFUR

LIQUID · CAPSICUM 3 [hp_X]/mL, FUCUS VESICULOSUS 3 [hp_X]/mL, BORAGE 6 [hp_X]/mL, EGG PHOSPHOLIPIDS 6 [hp_X]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL, IRON 12 [hp_X]/mL, POTASSIUM DICHROMATE 12 [hp_X]/mL, POTASSIUM CARBONATE 12 [hp_X]/mL, PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL, SULFUR 12 [hp_X]/mL

United StatesActive

Marketing holder: Energique, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • CAPSICUM · 3 [hp_X]/mL
  • FUCUS VESICULOSUS · 3 [hp_X]/mL
  • BORAGE · 6 [hp_X]/mL
  • EGG PHOSPHOLIPIDS · 6 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 12 [hp_X]/mL
  • IRON · 12 [hp_X]/mL
  • POTASSIUM DICHROMATE · 12 [hp_X]/mL
  • POTASSIUM CARBONATE · 12 [hp_X]/mL
  • PULSATILLA PRATENSIS WHOLE · 12 [hp_X]/mL
  • SULFUR · 12 [hp_X]/mL
Registration
Registration number
44911-0358
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 44911-0358 · Verified 2026-10-09 · open in source