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GUNA ARTHRO RELIEF

Wirkstoff: OYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM SULFATE, .ALPHA.-KETOGLUTARIC ACID, .ALPHA.-LIPOIC ACID, SUS SCROFA ARTERY, ASCORBIC ACID, BARIUM OXALOSUCCINATE, BRYONIA ALBA ROOT, SUS SCROFA CARTILAGE, CHLORINE, BLACK COHOSH, COLCHICUM AUTUMNALE BULB, SUS SCROFA EMBRYO, SOLANUM DULCAMARA FLOWER, SUS SCROFA UMBILICAL CORD, SUS SCROFA ADRENAL GLAND, NADIDE, SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA, TOXICODENDRON PUBESCENS LEAF, SULFUR, SUS SCROFA VEIN

Lösung / Tropfen [Übersetzung der Form; Original: SOLUTION/ DROPS (openFDA)] · OYSTER SHELL CALCIUM CARBONATE, CRUDE 4 [hp_X]/30mL, SODIUM SULFATE 8 [hp_X]/30mL, .ALPHA.-KETOGLUTARIC ACID 3 [hp_X]/30mL, .ALPHA.-LIPOIC ACID 8 [hp_X]/30mL, SUS SCROFA ARTERY 6 [hp_X]/30mL, ASCORBIC ACID 3 [hp_X]/30mL, BARIUM OXALOSUCCINATE 6 [hp_X]/30mL, BRYONIA ALBA ROOT 6 [hp_X]/30mL, SUS SCROFA CARTILAGE 6 [hp_X]/30mL, CHLORINE 6 [hp_X]/30mL, BLACK COHOSH 6 [hp_X]/30mL, COLCHICUM AUTUMNALE BULB 6 [hp_X]/30mL, SUS SCROFA EMBRYO 6 [hp_X]/30mL, SOLANUM DULCAMARA FLOWER 6 [hp_X]/30mL, SUS SCROFA UMBILICAL CORD 6 [hp_X]/30mL, SUS SCROFA ADRENAL GLAND 6 [hp_X]/30mL, NADIDE 3 [hp_X]/30mL, SODIUM DIETHYL OXALACETATE 3 [hp_X]/30mL, SUS SCROFA PLACENTA 6 [hp_X]/30mL, TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/30mL, SULFUR 4 [hp_X]/30mL, SUS SCROFA VEIN 6 [hp_X]/30mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Guna spa

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 4 [hp_X]/30mL
  • SODIUM SULFATE · 8 [hp_X]/30mL
  • .ALPHA.-KETOGLUTARIC ACID · 3 [hp_X]/30mL
  • .ALPHA.-LIPOIC ACID · 8 [hp_X]/30mL
  • SUS SCROFA ARTERY · 6 [hp_X]/30mL
  • ASCORBIC ACID · 3 [hp_X]/30mL
  • BARIUM OXALOSUCCINATE · 6 [hp_X]/30mL
  • BRYONIA ALBA ROOT · 6 [hp_X]/30mL
  • SUS SCROFA CARTILAGE · 6 [hp_X]/30mL
  • CHLORINE · 6 [hp_X]/30mL
  • BLACK COHOSH · 6 [hp_X]/30mL
  • COLCHICUM AUTUMNALE BULB · 6 [hp_X]/30mL
  • SUS SCROFA EMBRYO · 6 [hp_X]/30mL
  • SOLANUM DULCAMARA FLOWER · 6 [hp_X]/30mL
  • SUS SCROFA UMBILICAL CORD · 6 [hp_X]/30mL
  • SUS SCROFA ADRENAL GLAND · 6 [hp_X]/30mL
  • NADIDE · 3 [hp_X]/30mL
  • SODIUM DIETHYL OXALACETATE · 3 [hp_X]/30mL
  • SUS SCROFA PLACENTA · 6 [hp_X]/30mL
  • TOXICODENDRON PUBESCENS LEAF · 6 [hp_X]/30mL
  • SULFUR · 4 [hp_X]/30mL
  • SUS SCROFA VEIN · 6 [hp_X]/30mL
Zulassung
Zulassungsnummer
17089-463
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen