Dextrose Injection, Solution
Product Images NDC 63323-824

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 63323-824). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, 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

Dex0s 0002 01

Chemical structure diagram of Dextrose, shown as Dextrose Hydrous, USP (D-Glucose monohydrate). The diagram depicts the molecular arrangement including hydroxyl groups and water of hydration.*

FDA Label Image

Dex0s 0002 02

FDA Label Image

Dex0s 0002 03

Label for 10% Dextrose Injection, USP, 250 mL intravenous solution containing 25 grams of dextrose monohydrate per 250 mL (100 mg/mL) by Fresenius Kabi USA, LLC. The label includes usage instructions, storage conditions, pH, osmolality, and mentions that the single-dose container is sterile and non-PVC. Made in Germany.*

FDA Label Image

Dex0s 0002 04

Label for 10% Dextrose Injection, USP, 50 grams per 500 mL (100 mg/mL) intravenous injection solution by Fresenius Kabi USA, LLC. The label displays drug concentration, volume (500 mL), storage instructions, usage directions, and manufacturer information. It indicates the product is hypertonic and single-dose, with warnings about additives and container materials.*

FDA Label Image

Dex0s 0002 05

The packaging label for 10% Dextrose Injection, USP, containing 100 mg/mL of dextrose monohydrate as a solution for intravenous injection. The single-dose container holds 1,000 mL and is labeled for intravenous use only. The label includes storage instructions, manufacturer Fresenius Kabi USA, LLC, and specifies that the product is made in Germany. It notes the solution is hypertonic with pH 4.5 and includes a warning about additive incompatibility.*

* 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.