Label: MAGNESIUM SULFATE - magnesium sulfate injection, solution 

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 11/12

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  • Label
  • INGREDIENTS AND APPEARANCE
    MAGNESIUM SULFATE 
    magnesium sulfate injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:52533-099
    Route of Administration INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MAGNESIUM SULFATE (Magnesium Cation) MAGNESIUM SULFATE 20 g  in 500 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM CHLORIDE 3 g  in 500 mL
    SODIUM LACTATE 1.55 g  in 500 mL
    POTASSIUM CHLORIDE 0.15 g  in 500 mL
    CALCIUM CHLORIDE 0.1 g  in 500 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52533-099-29 500 mL in 1 BAG
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 02/21/2011
    Labeler - Cantrell Drug Company (035545763)
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