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GUNA-CELL

Wirkstoff: ACETYLCARNITINE, ADENOSINE CYCLIC PHOSPHATE, .ALPHA.-LIPOIC ACID, .ALPHA.-TOCOPHEROL ACETATE, DL-, ASCORBIC ACID, CALCIUM CARBONATE, CITRIC ACID MONOHYDRATE, COBALAMIN, COLCHICUM AUTUMNALE BULB, CONIUM MACULATUM FLOWERING TOP, CUPRIC SULFATE, HERRING SPERM DNA, FERROUS FUMARATE, FOLIC ACID, FUMARIC ACID, PYRUVALDEHYDE, POTASSIUM ASPARTATE, MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE, MANGANESE GLUCONATE, MANGANESE PHOSPHATE, DIBASIC, SODIUM DIETHYL OXALACETATE, SODIUM PYRUVATE, NIACIN, PANTOTHENIC ACID, PHOSPHORUS, PODOPHYLLUM PELTATUM ROOT, PYRIDOXINE HYDROCHLORIDE, RIBOFLAVIN, SACCHAROMYCES CEREVISIAE RNA, SELENOMETHIONINE, SUCCINIC ACID, SULFUR, THIAMINE HYDROCHLORIDE, ZINC

Lösung / Tropfen [Übersetzung der Form; Original: SOLUTION/ DROPS (openFDA)] · ACETYLCARNITINE 3 [hp_X]/30mL, ADENOSINE CYCLIC PHOSPHATE 6 [hp_X]/30mL, .ALPHA.-LIPOIC ACID 3 [hp_X]/30mL, .ALPHA.-TOCOPHEROL ACETATE, DL- 3 [hp_X]/30mL, ASCORBIC ACID 3 [hp_X]/30mL, CALCIUM CARBONATE 3 [hp_X]/30mL, CITRIC ACID MONOHYDRATE 3 [hp_X]/30mL, COBALAMIN 3 [hp_X]/30mL, COLCHICUM AUTUMNALE BULB 6 [hp_X]/30mL, CONIUM MACULATUM FLOWERING TOP 6 [hp_X]/30mL, CUPRIC SULFATE 3 [hp_X]/30mL, HERRING SPERM DNA 6 [hp_X]/30mL, FERROUS FUMARATE 3 [hp_X]/30mL, FOLIC ACID 3 [hp_X]/30mL, FUMARIC ACID 3 [hp_X]/30mL, PYRUVALDEHYDE 10 [hp_X]/30mL, POTASSIUM ASPARTATE 3 [hp_X]/30mL, MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE 3 [hp_X]/30mL, MANGANESE GLUCONATE 3 [hp_X]/30mL, MANGANESE PHOSPHATE, DIBASIC 6 [hp_X]/30mL, SODIUM DIETHYL OXALACETATE 3 [hp_X]/30mL, SODIUM PYRUVATE 3 [hp_X]/30mL, NIACIN 3 [hp_X]/30mL, PANTOTHENIC ACID 3 [hp_X]/30mL, PHOSPHORUS 4 [hp_X]/30mL, PODOPHYLLUM PELTATUM ROOT 6 [hp_X]/30mL, PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/30mL, RIBOFLAVIN 6 [hp_X]/30mL, SACCHAROMYCES CEREVISIAE RNA 6 [hp_X]/30mL, SELENOMETHIONINE 3 [hp_X]/30mL, SUCCINIC ACID 3 [hp_X]/30mL, SULFUR 3 [hp_X]/30mL, THIAMINE HYDROCHLORIDE 4 [hp_X]/30mL, ZINC 3 [hp_X]/30mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Guna spa

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
Zulassung
Zulassungsnummer
17089-450
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen