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Wirkstoff: SEMECARPUS ANACARDIUM JUICE, SODIUM TETRACHLOROAURATE, CAMPHOR (NATURAL), HERRING SPERM DNA, GERMANIUM, HELLEBORUS NIGER ROOT, HYDROGEN, CANIS LUPUS FAMILIARIS MILK, HUMAN MILK, LITHIUM CARBONATE, MAGNESIUM OXIDE, SODIUM CARBONATE, NEON, OXYTOCIN, SUS SCROFA PLACENTA, RHUS GLABRA TOP, SUCROSE, DATURA STRAMONIUM, THUJA OCCIDENTALIS LEAFY TWIG

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · SEMECARPUS ANACARDIUM JUICE 12 [hp_X]/mL, SODIUM TETRACHLOROAURATE 12 [hp_X]/mL, CAMPHOR (NATURAL) 12 [hp_X]/mL, HERRING SPERM DNA 12 [hp_X]/mL, GERMANIUM 15 [hp_X]/mL, HELLEBORUS NIGER ROOT 12 [hp_X]/mL, HYDROGEN 16 [hp_X]/mL, CANIS LUPUS FAMILIARIS MILK 10 [hp_X]/mL, HUMAN MILK 16 [hp_X]/mL, LITHIUM CARBONATE 8 [hp_X]/mL, MAGNESIUM OXIDE 12 [hp_X]/mL, SODIUM CARBONATE 6 [hp_X]/mL, NEON 16 [hp_C]/mL, OXYTOCIN 36 [hp_C]/mL, SUS SCROFA PLACENTA 8 [hp_X]/mL, RHUS GLABRA TOP 12 [hp_X]/mL, SUCROSE 6 [hp_X]/mL, DATURA STRAMONIUM 12 [hp_X]/mL, THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Deseret Biologicals, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • SEMECARPUS ANACARDIUM JUICE · 12 [hp_X]/mL
  • SODIUM TETRACHLOROAURATE · 12 [hp_X]/mL
  • CAMPHOR (NATURAL) · 12 [hp_X]/mL
  • HERRING SPERM DNA · 12 [hp_X]/mL
  • GERMANIUM · 15 [hp_X]/mL
  • HELLEBORUS NIGER ROOT · 12 [hp_X]/mL
  • HYDROGEN · 16 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS MILK · 10 [hp_X]/mL
  • HUMAN MILK · 16 [hp_X]/mL
  • LITHIUM CARBONATE · 8 [hp_X]/mL
  • MAGNESIUM OXIDE · 12 [hp_X]/mL
  • SODIUM CARBONATE · 6 [hp_X]/mL
  • NEON · 16 [hp_C]/mL
  • OXYTOCIN · 36 [hp_C]/mL
  • SUS SCROFA PLACENTA · 8 [hp_X]/mL
  • RHUS GLABRA TOP · 12 [hp_X]/mL
  • SUCROSE · 6 [hp_X]/mL
  • DATURA STRAMONIUM · 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG · 12 [hp_X]/mL
Zulassung
Zulassungsnummer
43742-2185
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen