Magnesium Sulfate Injection, Solution
Product Images NDC 72572-511

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate (NDC 72572-511). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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.

FDA Label Image

Magnesium Sulfate In Water Representative Container Label 72572-511-40 (Image 01)

Magnesium Sulfate In Water Representative Container Label 72572-511-40 (Image 01)
Label for Magnesium Sulfate 2 g/50 mL injection solution in water for injection by Civica, Inc. The label shows the product strength as 2 g total (40 mg/mL) in a 50 mL single-dose container for intravenous use. It includes storage instructions, manufacturer details (Baxter Healthcare Corporation), and warnings about usage and container materials.*
FDA Label Image

Magnesium Sulfate In Water Representative Overpouch Label 72572-511-40 (Image 02)

Magnesium Sulfate In Water Representative Overpouch Label 72572-511-40 (Image 02)
Magnesium Sulfate 2 g/50 mL (40 mg/mL) injection solution label for intravenous use. The label states the product contains Magnesium Sulfate Heptahydrate 2 g per 50 mL sterile, nonpyrogenic solution. It is a single-dose container with usage instructions, storage information, and manufacturing details by Baxter Healthcare Corp., distributed by Civica, Inc. The label includes dosage warnings and handling notes, with a barcode and QR code present.*

* 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.