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Wirkstoff: ACONITUM NAPELLUS WHOLE, SILVER NITRATE, ARSENIC TRIOXIDE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, HUMAN BREAST TUMOR CELL, CAUSTICUM, GELSEMIUM SEMPERVIRENS ROOT, LACHESIS MUTA VENOM, LITHIUM CARBONATE, LYCOPODIUM CLAVATUM SPORE, MERCURY, NITRIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF

Spray [Übersetzung der Form; Original: SPRAY (openFDA)] · ACONITUM NAPELLUS WHOLE 30 [hp_C]/mL, SILVER NITRATE 30 [hp_C]/mL, ARSENIC TRIOXIDE 30 [hp_C]/mL, ATROPA BELLADONNA 30 [hp_C]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL, HUMAN BREAST TUMOR CELL 30 [hp_C]/mL, CAUSTICUM 30 [hp_C]/mL, GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]/mL, LACHESIS MUTA VENOM 30 [hp_C]/mL, LITHIUM CARBONATE 30 [hp_C]/mL, LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL, MERCURY 30 [hp_C]/mL, NITRIC ACID 30 [hp_C]/mL, PHOSPHORUS 30 [hp_C]/mL, TOXICODENDRON PUBESCENS LEAF 30 [kp_C]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Energique, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • ACONITUM NAPELLUS WHOLE · 30 [hp_C]/mL
  • SILVER NITRATE · 30 [hp_C]/mL
  • ARSENIC TRIOXIDE · 30 [hp_C]/mL
  • ATROPA BELLADONNA · 30 [hp_C]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 30 [hp_C]/mL
  • HUMAN BREAST TUMOR CELL · 30 [hp_C]/mL
  • CAUSTICUM · 30 [hp_C]/mL
  • GELSEMIUM SEMPERVIRENS ROOT · 30 [hp_C]/mL
  • LACHESIS MUTA VENOM · 30 [hp_C]/mL
  • LITHIUM CARBONATE · 30 [hp_C]/mL
  • LYCOPODIUM CLAVATUM SPORE · 30 [hp_C]/mL
  • MERCURY · 30 [hp_C]/mL
  • NITRIC ACID · 30 [hp_C]/mL
  • PHOSPHORUS · 30 [hp_C]/mL
  • TOXICODENDRON PUBESCENS LEAF · 30 [kp_C]/mL
Zulassung
Zulassungsnummer
44911-0685
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen