Hospira Logo (Magnesium 01)
Magnesium Sulfate Injection, Solution
Product Images NDC 0409-2168
4 FDA label images from Hospira, Inc. · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate (NDC 0409-2168). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hospira, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Hospira Logo (Magnesium 02)
Principal Display Panel (20 mL Vial Label)
Label for Magnesium Sulfate Injection USP 50% solution at 0.5 g/mL (10 g/20 mL), indicated for intravenous or intramuscular use. The label includes caution for dilution before intravenous use, dosage information, and storage instructions. Distributed by Hospira, Inc., Lake Forest, IL. Contains NDC 0409-2168-17 with lot and expiration date placeholders.*
Principal Display Panel (20 mL Vial Tray)
Magnesium Sulfate Injection USP 50% 10 g/20 mL (0.5 g/mL) solution in a 20 mL single-use Fliptop vial. The label highlights its use for intravenous or intramuscular administration and includes a caution that the product must be diluted for intravenous use. It is distributed by Hospira, Inc. and contains NDC codes 0409-2168-77 and 0409-2168-17.*
* 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.
