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EyeClear Pro

Wirkstoff: NAPHTHALENE, CAUSTICUM, CALCIUM FLUORIDE, SENECIO VULGARIS, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SILICON DIOXIDE, SODIUM CHLORIDE, PHOSPHORUS, EUPHRASIA STRICTA, QUASSIA AMARA WOOD

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · NAPHTHALENE 30 [hp_X]/59mL, CAUSTICUM 30 [hp_X]/59mL, CALCIUM FLUORIDE 30 [hp_X]/59mL, SENECIO VULGARIS 30 [hp_X]/59mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/59mL, SILICON DIOXIDE 30 [hp_X]/59mL, SODIUM CHLORIDE 30 [hp_X]/59mL, PHOSPHORUS 30 [hp_X]/59mL, EUPHRASIA STRICTA 30 [hp_X]/59mL, QUASSIA AMARA WOOD 30 [hp_X]/59mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Silver Star Brands

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • NAPHTHALENE · 30 [hp_X]/59mL
  • CAUSTICUM · 30 [hp_X]/59mL
  • CALCIUM FLUORIDE · 30 [hp_X]/59mL
  • SENECIO VULGARIS · 30 [hp_X]/59mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 30 [hp_X]/59mL
  • SILICON DIOXIDE · 30 [hp_X]/59mL
  • SODIUM CHLORIDE · 30 [hp_X]/59mL
  • PHOSPHORUS · 30 [hp_X]/59mL
  • EUPHRASIA STRICTA · 30 [hp_X]/59mL
  • QUASSIA AMARA WOOD · 30 [hp_X]/59mL
Zulassung
Zulassungsnummer
68703-387
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen