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Sinus Congestion Headache

Wirkstoff: ANTIMONY POTASSIUM TARTRATE, FERULA ASSA-FOETIDA RESIN, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, EUPATORIUM PERFOLIATUM FLOWERING TOP, EUPHORBIA HIRTA FLOWERING TOP, CALCIUM SULFIDE, GOLDENSEAL, IODINE, POTASSIUM DICHROMATE, LACHESIS MUTA VENOM, MAGNESIUM CARBONATE, SUS SCROFA NASAL MUCOSA, PULSATILLA PRATENSIS WHOLE, RANCID BEEF, SILICON DIOXIDE, TEUCRIUM MARUM WHOLE

Spray [Übersetzung der Form; Original: SPRAY (openFDA)] · ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/mL, FERULA ASSA-FOETIDA RESIN 30 [hp_C]/mL, BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL, ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL, EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X]/mL, EUPHORBIA HIRTA FLOWERING TOP 6 [hp_X]/mL, CALCIUM SULFIDE 30 [hp_X]/mL, GOLDENSEAL 30 [hp_C]/mL, IODINE 200 [hp_C]/mL, POTASSIUM DICHROMATE 30 [hp_X]/mL, LACHESIS MUTA VENOM 200 [hp_C]/mL, MAGNESIUM CARBONATE 10 [hp_X]/mL, SUS SCROFA NASAL MUCOSA 12 [hp_X]/mL, PULSATILLA PRATENSIS WHOLE 30 [hp_C]/mL, RANCID BEEF 200 [hp_C]/mL, SILICON DIOXIDE 30 [hp_C]/mL, TEUCRIUM MARUM WHOLE 3 [hp_X]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Liddell Laboratories, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • ANTIMONY POTASSIUM TARTRATE · 6 [hp_X]/mL
  • FERULA ASSA-FOETIDA RESIN · 30 [hp_C]/mL
  • BAPTISIA TINCTORIA ROOT · 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA WHOLE · 3 [hp_X]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP · 6 [hp_X]/mL
  • EUPHORBIA HIRTA FLOWERING TOP · 6 [hp_X]/mL
  • CALCIUM SULFIDE · 30 [hp_X]/mL
  • GOLDENSEAL · 30 [hp_C]/mL
  • IODINE · 200 [hp_C]/mL
  • POTASSIUM DICHROMATE · 30 [hp_X]/mL
  • LACHESIS MUTA VENOM · 200 [hp_C]/mL
  • MAGNESIUM CARBONATE · 10 [hp_X]/mL
  • SUS SCROFA NASAL MUCOSA · 12 [hp_X]/mL
  • PULSATILLA PRATENSIS WHOLE · 30 [hp_C]/mL
  • RANCID BEEF · 200 [hp_C]/mL
  • SILICON DIOXIDE · 30 [hp_C]/mL
  • TEUCRIUM MARUM WHOLE · 3 [hp_X]/mL
Zulassung
Zulassungsnummer
50845-0263
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen