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RPT-Sys

Wirkstoff: TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, THYROID, UNSPECIFIED, TRILLIUM ERECTUM ROOT, APOCYNUM CANNABINUM ROOT, ASAFETIDA, SODIUM BORATE, EUCALYPTUS GLOBULUS LEAF, GENTIANA LUTEA ROOT, STRYCHNOS IGNATII SEED, WOOD CREOSOTE, LATHYRUS SATIVAS SEED, EGG PHOSPHOLIPIDS, LYCOPODIUM CLAVATUM SPORE, NUTMEG, OXALIC ACID DIHYDRATE, PHOSPHORIC ACID, SUS SCROFA PITUITARY GLAND, PLATINUM

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/mL, SILICON DIOXIDE 10 [hp_X]/mL, THYROID, UNSPECIFIED 6 [hp_C]/mL, TRILLIUM ERECTUM ROOT 3 [hp_X]/mL, APOCYNUM CANNABINUM ROOT 10 [hp_X]/mL, ASAFETIDA 6 [hp_X]/mL, SODIUM BORATE 7 [hp_X]/mL, EUCALYPTUS GLOBULUS LEAF 7 [hp_X]/mL, GENTIANA LUTEA ROOT 7 [hp_X]/mL, STRYCHNOS IGNATII SEED 10 [hp_X]/mL, WOOD CREOSOTE 8 [hp_X]/mL, LATHYRUS SATIVAS SEED 20 [hp_X]/mL, EGG PHOSPHOLIPIDS 20 [hp_X]/mL, LYCOPODIUM CLAVATUM SPORE 7 [hp_X]/mL, NUTMEG 7 [hp_X]/mL, OXALIC ACID DIHYDRATE 10 [hp_X]/mL, PHOSPHORIC ACID 8 [hp_X]/mL, SUS SCROFA PITUITARY GLAND 6 [hp_C]/mL, PLATINUM 10 [hp_X]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Vitality Works, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • TOXICODENDRON PUBESCENS LEAF · 10 [hp_X]/mL
  • SILICON DIOXIDE · 10 [hp_X]/mL
  • THYROID, UNSPECIFIED · 6 [hp_C]/mL
  • TRILLIUM ERECTUM ROOT · 3 [hp_X]/mL
  • APOCYNUM CANNABINUM ROOT · 10 [hp_X]/mL
  • ASAFETIDA · 6 [hp_X]/mL
  • SODIUM BORATE · 7 [hp_X]/mL
  • EUCALYPTUS GLOBULUS LEAF · 7 [hp_X]/mL
  • GENTIANA LUTEA ROOT · 7 [hp_X]/mL
  • STRYCHNOS IGNATII SEED · 10 [hp_X]/mL
  • WOOD CREOSOTE · 8 [hp_X]/mL
  • LATHYRUS SATIVAS SEED · 20 [hp_X]/mL
  • EGG PHOSPHOLIPIDS · 20 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE · 7 [hp_X]/mL
  • NUTMEG · 7 [hp_X]/mL
  • OXALIC ACID DIHYDRATE · 10 [hp_X]/mL
  • PHOSPHORIC ACID · 8 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND · 6 [hp_C]/mL
  • PLATINUM · 10 [hp_X]/mL
Zulassung
Zulassungsnummer
64616-104
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen