MAGNESIUM SULFATE  - magnesium sulfate injection, solution 
Cantrell Drug Company

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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MAGNESIUM SULFATE  magnesium injection, solution

Product Information Product Type HUMAN PRESCRIPTION DRUG 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 Cation 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

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:52533-099-29 500 mL in 1 BAG None

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)

Revised: 08/2012 Cantrell Drug Company