Mannitol Injection, Solution
Product Images NDC 0264-7578

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Mannitol (NDC 0264-7578). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by B. Braun Medical 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

Chemical Structure (Mannitol Injection Usp In Excel 1)

Chemical structure of Mannitol, a sugar alcohol used as the active ingredient in the injection solution form of this prescription drug.*

FDA Label Image

Other Symbol (Mannitol Injection Usp In Excel 2)

FDA Label Image

500 mL Container Label L5781 (Mannitol Injection Usp In Excel 3)

Label for Mannitol 20% Injection USP, 500 mL solution for intravenous use. The label specifies 20 g/100 mL concentration, contained in an EXCEL container by B. Braun Medical Inc. It includes warnings about sterility, use instructions, storage conditions at room temperature, and cautions against admixing with other drugs and use of natural rubber latex, PVC, or DEHP materials.*

FDA Label Image

Other Symbol (Mannitol Injection Usp In Excel 4)

FDA Label Image

250 mL Container Label L5782 (Mannitol Injection Usp In Excel 5)

Label for Mannitol 20% Injection USP, 250 mL intravenous solution by B. Braun Medical Inc. Each 100 mL contains 20 g Mannitol. The label includes reference number L5782, NDC 0264-7578-20, and container volume. It provides usage instructions, warnings, storage conditions, and manufacturer information. The label also features the B. Braun logo and barcode areas.*

* 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.