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Vertigo Syncope Drops 2115

Wirkstoff: ARNICA MONTANA WHOLE, CENTELLA ASIATICA LEAF, PHOSPHORIC ACID, AMBERGRIS, SILVER NITRATE, ANAMIRTA COCCULUS FRUIT, CONIUM MACULATUM FLOWERING TOP, CANIS LUPUS FAMILIARIS MILK, THERIDION CURASSAVICUM

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · ARNICA MONTANA WHOLE 3 [hp_X]/59mL, CENTELLA ASIATICA LEAF 3 [hp_X]/59mL, PHOSPHORIC ACID 6 [hp_X]/59mL, AMBERGRIS 12 [hp_X]/59mL, SILVER NITRATE 12 [hp_X]/59mL, ANAMIRTA COCCULUS FRUIT 12 [hp_X]/59mL, CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/59mL, CANIS LUPUS FAMILIARIS MILK 12 [hp_X]/59mL, THERIDION CURASSAVICUM 12 [hp_X]/59mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Professional Complementary Health Formulas

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • ARNICA MONTANA WHOLE · 3 [hp_X]/59mL
  • CENTELLA ASIATICA LEAF · 3 [hp_X]/59mL
  • PHOSPHORIC ACID · 6 [hp_X]/59mL
  • AMBERGRIS · 12 [hp_X]/59mL
  • SILVER NITRATE · 12 [hp_X]/59mL
  • ANAMIRTA COCCULUS FRUIT · 12 [hp_X]/59mL
  • CONIUM MACULATUM FLOWERING TOP · 12 [hp_X]/59mL
  • CANIS LUPUS FAMILIARIS MILK · 12 [hp_X]/59mL
  • THERIDION CURASSAVICUM · 12 [hp_X]/59mL
Zulassung
Zulassungsnummer
63083-2115
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen