Dextrose Injection, Solution
Product Images NDC 0990-7120

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 0990-7120). 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

Dextrose Structural Formula (Dextrose 01)

Dextrose Structural Formula (Dextrose 01)
Chemical structure of dextrose monohydrate showing the molecular ring with multiple hydroxyl groups and an attached water molecule (H2O).*
FDA Label Image

Principal Display Panel (70 g Bag Label)

Principal Display Panel (70 g Bag Label)
Label for Dextrose Injection USP 70% (70 g/100 mL) in a 2000 mL pharmacy bulk package by ICU Medical Inc. The label states that the solution is hypertonic and must be diluted, not for direct infusion. Instructions include storage conditions, usage cautions, and sterility information. The label also features the NDC 0990-7120-07, latex-free and DEHP content symbols, and the ICU Medical logo.*
FDA Label Image

Principal Display Panel (70 g Bag Overwrap Label)

Principal Display Panel (70 g Bag Overwrap Label)
Label text panel for Dextrose injection solution by ICU Medical Inc., providing storage and handling instructions. It advises tearing at the notch to open, inspecting the overwrap for integrity, storing at controlled room temperature (20 to 25°C), protecting from freezing, and discarding if leaks are found. It notes that color variation from pale yellow to yellow is normal and does not affect efficacy. The label includes a barcode and the manufacturer's address in Lake Forest, Illinois.*

* 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.