Label: MAGNESIUM CHLORIDE- magnesium chloride injection

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

Drug Label Information

Updated 03/13

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    PRINCIPAL DISPLAY PANEL - 200 mg/mL
    NDC 67457-134-50     50 mL

    Magnesium Chloride Injection 200 mg/mL (20 percent w/v) Carton Label
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  • INGREDIENTS AND APPEARANCE
    MAGNESIUM CHLORIDE 
    magnesium chloride injection
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:63286-0134
    Route of Administration INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MAGNESIUM CHLORIDE (MAGNESIUM CATION) MAGNESIUM CHLORIDE 200 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE 9 mg  in 1 mL
    BENZYL ALCOHOL 10 mg  in 1 mL
    WATER  
    HYDROCHLORIC ACID  
    SODIUM HYDROXIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63286-0134-5 1 in 1 CARTON
    1 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved drug other 03/14/2013
    Labeler - Mylan Teoranta (896321325)
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