Dextrose Injection, Solution
Product Images NDC 0990-7922

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 0990-7922). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Icu 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

Principal Display Panel (100 mL Bag Label)

Label for 5% Dextrose Injection, USP, presenting a 100 mL single-dose container. The label highlights the active ingredient as 5 g hydrous dextrose per 100 mL. Additional visible information includes the labeler ICU Medical Inc., Latex content, DEHP presence, and usage warnings related to solution clarity and container integrity.*

FDA Label Image

Principal Display Panel (250 mL Bag Label)

Label for 5% Dextrose Injection, USP in a 250 mL container. The label lists the active ingredient as 5 g dextrose in water for injection per 100 mL. It includes usage instructions, warnings about additives and compatibility, and indicates the product is sterile, nonpyrogenic, and for intravenous use only. Manufactured for ICU Medical Inc. in Lake Forest, Illinois.*

FDA Label Image

Principal Display Panel (500 mL Bag Label)

Label for 10% Dextrose Injection, USP, 10 g/100 mL strength in a 500 mL container. The label states the product contains dextrose, hydrous, in water for injection, with pH 4.3 and no salts. It is sterile, nonpyrogenic, single-dose, for intravenous or subcutaneous use, and manufactured by ICU Medical Inc.*

FDA Label Image

Structural Formula Dextrose (Dextrose Injection Usp3 Figure 1 Xen 1072 1)

Chemical structure of Dextrose with the addition of one water molecule (H2O), indicating a hydrated form of the molecule.*

* 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.