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Low Vaccinosis Nosode 4024

Wirkstoff: OYSTER SHELL CALCIUM CARBONATE, CRUDE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAF, LAURTRIMONIUM BROMIDE, MUMPS VIRUS, CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED), ANGUILLA ROSTRATA BLOOD SERUM, SERUM, HORSE

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_X]/59mL, SILICON DIOXIDE 6 [hp_X]/59mL, THUJA OCCIDENTALIS LEAF 6 [hp_X]/59mL, LAURTRIMONIUM BROMIDE 9 [hp_X]/59mL, MUMPS VIRUS 9 [hp_X]/59mL, CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) 9 [hp_X]/59mL, ANGUILLA ROSTRATA BLOOD SERUM 12 [hp_X]/59mL, SERUM, HORSE 12 [hp_X]/59mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Professional Complementary Health Formulas

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 6 [hp_X]/59mL
  • SILICON DIOXIDE · 6 [hp_X]/59mL
  • THUJA OCCIDENTALIS LEAF · 6 [hp_X]/59mL
  • LAURTRIMONIUM BROMIDE · 9 [hp_X]/59mL
  • MUMPS VIRUS · 9 [hp_X]/59mL
  • CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) · 9 [hp_X]/59mL
  • ANGUILLA ROSTRATA BLOOD SERUM · 12 [hp_X]/59mL
  • SERUM, HORSE · 12 [hp_X]/59mL
Zulassung
Zulassungsnummer
63083-4024
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen