Dextrose Injection, Solution
Product Images NDC 70518-4219

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 70518-4219). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Dextrose 50 25g 50ml(0.5g mL) 70518 4219 01)

Mm2 (Dextrose 50 25g  50ml(0.5g mL) 70518 4219 01)
Label for Dextrose 50% injection solution, containing 25 g per 50 mL (0.5 g/mL) in a prefilled 50 mL syringe. The product is labeled by RemedyRepack Inc. and notes the source manufacturer as Hospira, Inc., Lake Forest, IL. The label includes storage instructions, safety warnings, and a barcode with an NDC number 70518-4219-01.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Label for Dextrose 50% injection, 25 g/50 mL solution in prefilled syringes. The package contains 10 syringes of 50 mL each. The product is labeled for intravenous use and repackaged by RemedyRepack Inc. The label includes a barcode, NDC number 70518-4219-00, and manufacturer information (Hospira, Inc., Lake Forest, IL). Warnings and storage instructions are also visible.*
FDA Label Image

Chemical Structure (Dextrose 01)

Chemical Structure (Dextrose 01)
Chemical structure of Dextrose Monohydrate showing the glucose ring with hydroxyl groups and a single molecule of water (H2O) indicated alongside, representing the monohydrate form.*

* 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.