Magnesium Sulfate Injection, Solution
Product Images NDC 51662-1373

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate (NDC 51662-1373). 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.

FDA Label Image

Bag Label (Bag Label)

Label for Magnesium Sulfate injection, solution in water for injection, 2 g total in 50 mL (40 mg/mL) for intravenous infusion. The label includes detailed drug content information, pH, osmolality, and manufacturing details by Fresenius Kabi USA, LLC. It notes the product is Rx only and mentions that the bag is free of natural rubber latex, PVC, and DEHP.*

FDA Label Image

How Supplied (How Supplied)

A data table presenting different product codes, units of sale, total magnesium sulfate content, magnesium ion concentration, magnesium sulfate concentration, osmolarity (calculated), and unit of use details for various magnesium sulfate injection solutions. Concentrations range from 4% to 8%, with osmolarity values around 325 and 649 mOsmol/L, packaged primarily in Freeflex Bags of 50 mL, 100 mL, 500 mL, and 1,000 mL sizes.*

FDA Label Image

Logo (Logo)

FDA Label Image

Serialized Labeling (Serialized Bag Resized)

Magnesium Sulfate 40 mg/mL injection solution for intravenous use in a clear plastic bag. The label states 2 g total in 50 mL and includes manufacturer details: Fresenius Kabi USA, LLC, distributed by HF Acquisition Co., LLC. The packaging is a single-use sterile unit with a blue cap visible inside the sealed bag.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.