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GLUCOREKT

Active substance: LACTIC ACID, DL-, SULFURIC ACID, ONION, CHIONANTHUS VIRGINICUS ROOT BARK, PHOSPHORUS, ZINC SULFATE HEPTAHYDRATE, CORN SILK, SYZYGIUM CUMINI FRUIT

SOLUTION/ DROPS · LACTIC ACID, DL- 6 [hp_X]/50mL, SULFURIC ACID 6 [hp_X]/50mL, ONION 4 [hp_X]/50mL, CHIONANTHUS VIRGINICUS ROOT BARK 3 [hp_X]/50mL, PHOSPHORUS 10 [hp_X]/50mL, ZINC SULFATE HEPTAHYDRATE 3 [hp_X]/50mL, CORN SILK 669 mg/50mL, SYZYGIUM CUMINI FRUIT 3 [hp_X]/50mL

United StatesActive

Marketing holder: PEKANA Naturheilmittel GmbH

Verified 2026-10-09 · openFDA NDC

Composition
  • LACTIC ACID, DL- · 6 [hp_X]/50mL
  • SULFURIC ACID · 6 [hp_X]/50mL
  • ONION · 4 [hp_X]/50mL
  • CHIONANTHUS VIRGINICUS ROOT BARK · 3 [hp_X]/50mL
  • PHOSPHORUS · 10 [hp_X]/50mL
  • ZINC SULFATE HEPTAHYDRATE · 3 [hp_X]/50mL
  • CORN SILK · 669 mg/50mL
  • SYZYGIUM CUMINI FRUIT · 3 [hp_X]/50mL
Registration
Registration number
59469-308
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 59469-308 · Verified 2026-10-09 · open in source