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Ear Ring

Wirkstoff: ONION, SILVER NITRATE, ASARUM CANADENSE ROOT, ACTIVATED CHARCOAL, CARBON DISULFIDE, SUS SCROFA CARTILAGE, DYSPHANIA AMBROSIOIDES WHOLE, QUININE SULFATE, CYCLAMEN PURPURASCENS TUBER, SOLANUM DULCAMARA TOP, GINKGO, GRAPHITE, WOOD CREOSOTE, SUS SCROFA NASAL MUCOSA, SODIUM SALICYLATE, PHOSPHORUS, LEAD, THERIDION CURASSAVICUM, ZINC

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · ONION 6 [hp_X]/mL, SILVER NITRATE 6 [hp_X]/mL, ASARUM CANADENSE ROOT 9 [hp_X]/mL, ACTIVATED CHARCOAL 12 [hp_X]/mL, CARBON DISULFIDE 12 [hp_X]/mL, SUS SCROFA CARTILAGE 8 [hp_X]/mL, DYSPHANIA AMBROSIOIDES WHOLE 6 [hp_X]/mL, QUININE SULFATE 6 [hp_X]/mL, CYCLAMEN PURPURASCENS TUBER 12 [hp_X]/mL, SOLANUM DULCAMARA TOP 6 [hp_X]/mL, GINKGO 6 [hp_X]/mL, GRAPHITE 12 [hp_X]/mL, WOOD CREOSOTE 12 [hp_X]/mL, SUS SCROFA NASAL MUCOSA 8 [hp_X]/mL, SODIUM SALICYLATE 10 [hp_X]/mL, PHOSPHORUS 12 [hp_X]/mL, LEAD 12 [hp_X]/mL, THERIDION CURASSAVICUM 12 [hp_X]/mL, ZINC 12 [hp_X]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Deseret Biologicals, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • ONION · 6 [hp_X]/mL
  • SILVER NITRATE · 6 [hp_X]/mL
  • ASARUM CANADENSE ROOT · 9 [hp_X]/mL
  • ACTIVATED CHARCOAL · 12 [hp_X]/mL
  • CARBON DISULFIDE · 12 [hp_X]/mL
  • SUS SCROFA CARTILAGE · 8 [hp_X]/mL
  • DYSPHANIA AMBROSIOIDES WHOLE · 6 [hp_X]/mL
  • QUININE SULFATE · 6 [hp_X]/mL
  • CYCLAMEN PURPURASCENS TUBER · 12 [hp_X]/mL
  • SOLANUM DULCAMARA TOP · 6 [hp_X]/mL
  • GINKGO · 6 [hp_X]/mL
  • GRAPHITE · 12 [hp_X]/mL
  • WOOD CREOSOTE · 12 [hp_X]/mL
  • SUS SCROFA NASAL MUCOSA · 8 [hp_X]/mL
  • SODIUM SALICYLATE · 10 [hp_X]/mL
  • PHOSPHORUS · 12 [hp_X]/mL
  • LEAD · 12 [hp_X]/mL
  • THERIDION CURASSAVICUM · 12 [hp_X]/mL
  • ZINC · 12 [hp_X]/mL
Zulassung
Zulassungsnummer
43742-2264
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen