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

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

Vereinigte StaatenAktiv

Zulassungsinhaber: Deseret Biologicals, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • SODIUM CARBONATE · 6 [hp_X]/mL
  • SUCROSE · 6 [hp_X]/mL
  • LITHIUM CARBONATE · 8 [hp_X]/mL
  • SUS SCROFA PLACENTA · 8 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS MILK · 10 [hp_X]/mL
  • SEMECARPUS ANACARDIUM JUICE · 12 [hp_X]/mL
  • SODIUM TETRACHLOROAURATE · 12 [hp_X]/mL
  • CAMPHOR (NATURAL) · 12 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE · 12 [hp_X]/mL
  • HELLEBORUS NIGER ROOT · 12 [hp_X]/mL
  • MAGNESIUM OXIDE · 12 [hp_X]/mL
  • RHUS GLABRA TOP · 12 [hp_X]/mL
  • DATURA STRAMONIUM · 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG · 12 [hp_X]/mL
  • HERRING SPERM DNA · 12 [hp_X]/mL
  • OXYTOCIN · 12 [hp_X]/mL
  • HYDROGEN · 16 [hp_X]/mL
  • NEON · 16 [hp_X]/mL
  • HUMAN MILK · 16 [hp_X]/mL
Zulassung
Zulassungsnummer
43742-1620
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen