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Cell Well

Wirkstoff: OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, CALCIUM PHOSPHATE, UNSPECIFIED FORM, CALCIUM SULFATE, UNSPECIFIED FORM, FERROSOFERRIC PHOSPHATE, POTASSIUM CHLORIDE, POTASSIUM PHOSPHATE, UNSPECIFIED FORM, POTASSIUM SULFATE, MAGNESIUM CARBONATE, MAGNESIUM PHOSPHATE ANHYDROUS, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM SULFATE, SILICON DIOXIDE

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_X]/60mL, CALCIUM FLUORIDE 6 [hp_X]/60mL, CALCIUM PHOSPHATE, UNSPECIFIED FORM 6 [hp_X]/60mL, CALCIUM SULFATE, UNSPECIFIED FORM 6 [hp_X]/60mL, FERROSOFERRIC PHOSPHATE 6 [hp_X]/60mL, POTASSIUM CHLORIDE 6 [hp_X]/60mL, POTASSIUM PHOSPHATE, UNSPECIFIED FORM 6 [hp_X]/60mL, POTASSIUM SULFATE 6 [hp_X]/60mL, MAGNESIUM CARBONATE 6 [hp_X]/60mL, MAGNESIUM PHOSPHATE ANHYDROUS 6 [hp_X]/60mL, SODIUM CHLORIDE 6 [hp_X]/60mL, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 6 [hp_Q]/60mL, SODIUM SULFATE 6 [hp_X]/60mL, SILICON DIOXIDE 6 [hp_Q]/60mL

Vereinigte StaatenAktiv

Zulassungsinhaber: JoyWell Co LLC

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
Zulassung
Zulassungsnummer
85946-0001
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen