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Scrofularoforce

Wirkstoff: RUMEX CRISPUS ROOT, ZANTHOXYLUM AMERICANUM BARK, SUS SCROFA LYMPH, SCROPHULARIA NODOSA WHOLE, BARIUM CARBONATE, BARIUM CHLORIDE DIHYDRATE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CONIUM MACULATUM FLOWERING TOP, HELLEBORUS NIGER ROOT, IODINE, DIBASIC POTASSIUM PHOSPHATE, LACHESIS MUTA VENOM, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SILICON DIOXIDE, JUNIPERUS VIRGINIANA TWIG

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · RUMEX CRISPUS ROOT 3 [hp_X]/mL, ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL, SUS SCROFA LYMPH 8 [hp_X]/mL, SCROPHULARIA NODOSA WHOLE 8 [hp_X]/mL, BARIUM CARBONATE 12 [hp_X]/mL, BARIUM CHLORIDE DIHYDRATE 12 [hp_X]/mL, ATROPA BELLADONNA 12 [hp_X]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL, CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL, HELLEBORUS NIGER ROOT 12 [hp_X]/mL, IODINE 12 [hp_X]/mL, DIBASIC POTASSIUM PHOSPHATE 12 [hp_X]/mL, LACHESIS MUTA VENOM 12 [hp_X]/mL, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/mL, SILICON DIOXIDE 12 [hp_X]/mL, JUNIPERUS VIRGINIANA TWIG 16 [hp_X]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: BioActive Nutritional, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • RUMEX CRISPUS ROOT · 3 [hp_X]/mL
  • ZANTHOXYLUM AMERICANUM BARK · 3 [hp_X]/mL
  • SUS SCROFA LYMPH · 8 [hp_X]/mL
  • SCROPHULARIA NODOSA WHOLE · 8 [hp_X]/mL
  • BARIUM CARBONATE · 12 [hp_X]/mL
  • BARIUM CHLORIDE DIHYDRATE · 12 [hp_X]/mL
  • ATROPA BELLADONNA · 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 12 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP · 12 [hp_X]/mL
  • HELLEBORUS NIGER ROOT · 12 [hp_X]/mL
  • IODINE · 12 [hp_X]/mL
  • DIBASIC POTASSIUM PHOSPHATE · 12 [hp_X]/mL
  • LACHESIS MUTA VENOM · 12 [hp_X]/mL
  • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE · 12 [hp_X]/mL
  • SILICON DIOXIDE · 12 [hp_X]/mL
  • JUNIPERUS VIRGINIANA TWIG · 16 [hp_X]/mL
Zulassung
Zulassungsnummer
43857-0580
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen