Magnesium Sulfate
Product Images NDC 51662-1451
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate (NDC 51662-1451). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hf Acquisition Co Llc, Dba Healthfirst, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
How Supplied (How Supplied)
Product details for Magnesium Sulfate are available in the table. This includes the National Drug Code (NDC), Fill No., Volume, and Magnesium Sulfate concentration in mg/mL and mag/mL. The NDC numbers for different variations of Magnesium Sulfate are 964003, 96402, 964011, and 96410P, each having a unique fill and volume.*
Logo (Logo)
Vial Label (New Vial Label)
This text describes a medication labeled as NDC 63323-06'1-04, which is an injection of Magnesium Sulfate USP that is intended for intramuscular or intravenous use. It has a strength of 5 grams per 10 mL and is provided in a 10 mL single-dose vial that must be diluted before intravenous use. The medication does not contain preservatives and is sterile. It includes magnesium sulfate heptahydrate 500 mg per mL and may contain sulfuric acid and/or sodium hydroxide for pH adjustment. The solution has 4.06 mEg/mL and 4.06 mOsmol/mL, and contains no more than 300 mcg/L of aluminum. The manufacturer is Fresenius Kabi based in Lake Zurich, IL. The text provides information about storage, dosage, discard, and prescription requirements. The package might contain a leaflet with more information.*
Serialized Label (Serialized Label)
This is a description of an injection in a single dose vial, containing Magnesium Sulfate, which is intended for intramuscular or intravenous use after dilution. It is preservative-free and each vial contains 5 grams per 107. It comes with a manufacturer's package insert and is distributed by HF Acquisition Co., based in Mukilteo, WA. The National Drug Code (NDC) for this product is 63323-064-04.*
Vial 3rd Part (Vial 3rd Part)
Vial 1st Part (Vial Label 1st Part)
This is a description of a medication called Magnesium Sulfate Injection, USP. It has an NDC code of 63323-064-04 and comes in a single dose vial of 10mL. It contains 5 grams of magnesium sulfate per 10mL (500mg per mL) and is intended for intramuscular or intravenous use. Before intravenous use, the medication must be diluted. It does not contain preservatives and must be stored properly. It is available only by prescription (Rx only).*
Vial 2nd Part (Vial Label 2nd Part)
This is a description of a sterile solution containing Magnesium sulphate heptahydrate (500mg per mL). The solution has been adjusted to the required pH with either Sulfuric acid or Sodium hydroxide. This solution is stored at temperatures between 20 and 25°C and is used for injection purposes only. The package insert should be referred to for the appropriate dosage. It also contains no more than 300mcg/L of aluminium. The solution is to be discarded if the seal is broken or the solution is not clear. The manufacturer is Fresenius Kabi.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.