Magnesium Sulfate In Dextrose Injection, Solution
Product Images NDC 0338-1709

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate In Dextrose (NDC 0338-1709). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Dextrose Structural Formula (Image 01)

Chemical structure of the active ingredient, magnesium sulfate in dextrose, showing the molecular arrangement of dextrose with an associated water molecule (H2O).*

FDA Label Image

Magnesium Sulfate In Dextrose Representative Container Label 0338-1709-40 (Image 02)

Label for Magnesium Sulfate in 5% Dextrose Injection USP, 1 g/100 mL (10 mg/mL) intravenous solution, 100 mL single-dose container. Label shows active ingredient strength, usage instructions including storage and handling precautions, manufacturer Baxter Healthcare Corporation, and product NDC 0338-1709-40.*

FDA Label Image

Image 03

MAGNESIUM SULFATE IN DEXTROSE 1 g/100 mL injection solution label by Baxter Healthcare Corporation. The label states the active ingredient as magnesium sulfate heptahydrate 1 g in 100 mL (10 mg/mL) in 5% dextrose, for intravenous use in a single-dose container. It includes storage instructions, pH range, warnings not to add supplementary medication, and the product NDC 0338-1709-40. The label also features a barcode and manufacturing details indicating it is made in Ireland.*

* 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.