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Lymph/Spleen Combo

Wirkstoff: ADENOSINE TRIPHOSPHATE DISODIUM, APIS MELLIFERA, CASTANEA SATIVA LEAF, CEANOTHUS AMERICANUS LEAF, QUININE ARSENITE, IRON, HELIANTHUS ANNUUS FLOWERING TOP, JUNIPER BERRY, SUS SCROFA LYMPH, MYOSOTIS ARVENSIS WHOLE, SODIUM CHLORIDE, SODIUM SULFATE, PHYTOLACCA AMERICANA ROOT, QUERCUS ROBUR NUT, SUS SCROFA SPLEEN, AMBER, SUS SCROFA THYMUS, UBIDECARENONE

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL, APIS MELLIFERA 200 [hp_C]/mL, CASTANEA SATIVA LEAF 6 [hp_C]/mL, CEANOTHUS AMERICANUS LEAF 6 [hp_X]/mL, QUININE ARSENITE 12 [hp_X]/mL, IRON 30 [hp_X]/mL, HELIANTHUS ANNUUS FLOWERING TOP 30 [hp_X]/mL, JUNIPER BERRY 3 [hp_X]/mL, SUS SCROFA LYMPH 8 [hp_X]/mL, MYOSOTIS ARVENSIS WHOLE 9 [hp_X]/mL, SODIUM CHLORIDE 6 [hp_X]/mL, SODIUM SULFATE 6 [hp_X]/mL, PHYTOLACCA AMERICANA ROOT 8 [hp_X]/mL, QUERCUS ROBUR NUT 6 [hp_X]/mL, SUS SCROFA SPLEEN 8 [hp_X]/mL, AMBER 30 [hp_X]/mL, SUS SCROFA THYMUS 8 [hp_X]/mL, UBIDECARENONE 12 [hp_X]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Deseret Biologicals, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • ADENOSINE TRIPHOSPHATE DISODIUM · 12 [hp_X]/mL
  • APIS MELLIFERA · 200 [hp_C]/mL
  • CASTANEA SATIVA LEAF · 6 [hp_C]/mL
  • CEANOTHUS AMERICANUS LEAF · 6 [hp_X]/mL
  • QUININE ARSENITE · 12 [hp_X]/mL
  • IRON · 30 [hp_X]/mL
  • HELIANTHUS ANNUUS FLOWERING TOP · 30 [hp_X]/mL
  • JUNIPER BERRY · 3 [hp_X]/mL
  • SUS SCROFA LYMPH · 8 [hp_X]/mL
  • MYOSOTIS ARVENSIS WHOLE · 9 [hp_X]/mL
  • SODIUM CHLORIDE · 6 [hp_X]/mL
  • SODIUM SULFATE · 6 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT · 8 [hp_X]/mL
  • QUERCUS ROBUR NUT · 6 [hp_X]/mL
  • SUS SCROFA SPLEEN · 8 [hp_X]/mL
  • AMBER · 30 [hp_X]/mL
  • SUS SCROFA THYMUS · 8 [hp_X]/mL
  • UBIDECARENONE · 12 [hp_X]/mL
Zulassung
Zulassungsnummer
43742-2176
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen