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Bio Placenta Phase

Wirkstoff: HORSE CHESTNUT, LACTIC ACID, L-, CUPRIC SULFATE, MELILOTUS OFFICINALIS TOP, SUS SCROFA PLACENTA, SOLANUM NIGRUM WHOLE, STROPHANTHUS HISPIDUS SEED, PRASTERONE, QUERCETIN, RUTIN, SODIUM PYRUVATE, CLAVICEPS PURPUREA SCLEROTIUM, SUS SCROFA VEIN, SUS SCROFA ARTERY, SUS SCROFA UMBILICAL CORD, TOBACCO LEAF, BARIUM CARBONATE, VIPERA BERUS VENOM, LEAD IODIDE, ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING, PROTEUS VULGARIS

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · HORSE CHESTNUT 4 [hp_X]/mL, LACTIC ACID, L- 4 [hp_X]/mL, CUPRIC SULFATE 6 [hp_X]/mL, MELILOTUS OFFICINALIS TOP 6 [hp_X]/mL, SUS SCROFA PLACENTA 6 [hp_X]/mL, SOLANUM NIGRUM WHOLE 6 [hp_X]/mL, STROPHANTHUS HISPIDUS SEED 6 [hp_X]/mL, PRASTERONE 6 [hp_X]/mL, QUERCETIN 6 [hp_X]/mL, RUTIN 6 [hp_X]/mL, SODIUM PYRUVATE 8 [hp_X]/mL, CLAVICEPS PURPUREA SCLEROTIUM 8 [hp_X]/mL, SUS SCROFA VEIN 8 [hp_X]/mL, SUS SCROFA ARTERY 10 [hp_X]/mL, SUS SCROFA UMBILICAL CORD 10 [hp_X]/mL, TOBACCO LEAF 10 [hp_X]/mL, BARIUM CARBONATE 13 [hp_X]/mL, VIPERA BERUS VENOM 14 [hp_X]/mL, LEAD IODIDE 18 [hp_X]/mL, ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING 6 [hp_C]/mL, PROTEUS VULGARIS 30 [hp_C]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Deseret Biologicals, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • HORSE CHESTNUT · 4 [hp_X]/mL
  • LACTIC ACID, L- · 4 [hp_X]/mL
  • CUPRIC SULFATE · 6 [hp_X]/mL
  • MELILOTUS OFFICINALIS TOP · 6 [hp_X]/mL
  • SUS SCROFA PLACENTA · 6 [hp_X]/mL
  • SOLANUM NIGRUM WHOLE · 6 [hp_X]/mL
  • STROPHANTHUS HISPIDUS SEED · 6 [hp_X]/mL
  • PRASTERONE · 6 [hp_X]/mL
  • QUERCETIN · 6 [hp_X]/mL
  • RUTIN · 6 [hp_X]/mL
  • SODIUM PYRUVATE · 8 [hp_X]/mL
  • CLAVICEPS PURPUREA SCLEROTIUM · 8 [hp_X]/mL
  • SUS SCROFA VEIN · 8 [hp_X]/mL
  • SUS SCROFA ARTERY · 10 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD · 10 [hp_X]/mL
  • TOBACCO LEAF · 10 [hp_X]/mL
  • BARIUM CARBONATE · 13 [hp_X]/mL
  • VIPERA BERUS VENOM · 14 [hp_X]/mL
  • LEAD IODIDE · 18 [hp_X]/mL
  • ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING · 6 [hp_C]/mL
  • PROTEUS VULGARIS · 30 [hp_C]/mL
Zulassung
Zulassungsnummer
43742-1954
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen