Dextrose Injection, Solution
Product Images NDC 0404-9845

3 FDA label images from Henry Schein, Inc. · 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 0404-9845). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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.

Product Images & Figures Index

FDA Label Image

Formula1.jpg (Formula1)

Formula1.jpg (Formula1)
Chemical structure of Dextrose Monohydrate, showing the molecular ring with attached hydroxyl groups and one water molecule (H2O) indicating the monohydrate form.*
FDA Label Image

Image1.jpg (Image1)

Image1.jpg (Image1)
A data table listing units of sale and concentration for Dextrose 25 g/50 mL injection solution. It includes bundles of 10 LifeShield Abboject Unit of Use Syringes with male luer, trays of 25 50 mL single-dose fliptop vials, and bundles of 10 Ansyr II plastic syringes with syringe and barrel detached. Concentration is noted as 0.5 g/mL.*
FDA Label Image

Label1.jpg (Label1)

Label1.jpg (Label1)
Label for Dextrose 25 g/50 mL Injection, USP, a unit of use syringe for intravenous administration. The label states 50% Dextrose with 0.5 g/mL concentration in a 56 mL volume. It includes storage instructions at controlled room temperature (20 to 25°C), single-dose use warning, and a caution to keep out of children's reach. Packaged by Henry Schein, Inc., located in Bastian, VA. The label features an NDC barcode (0404-9845-50) and area for lot and expiration date information, marked as RX ONLY.*

* 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.