Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 63323-874

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 63323-874). 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

Structural Formula (Dex0x 0001 01)

Structural Formula (Dex0x 0001 01)
Chemical structure of D-Glucose monohydrate, the active ingredient in Dextrose and Sodium Chloride injection solution.*
FDA Label Image

Logo (Dex0x 0001 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY –2.5% Dextrose and 0.45% Sodium)

Package Label (PRINCIPAL DISPLAY –2.5% Dextrose and 0.45% Sodium)
Label for 2.5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL intravenous solution by Fresenius Kabi USA, LLC. The single-dose container contains dextrose 2.5 g and sodium chloride 450 mg per 100 mL, with specified electrolytes and pH. The label advises storage at 20° to 25°C and notes packaging details including non-latex closure and non-PVC material.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 2.5% Dextrose and 0.45%)

Package Label (PRINCIPAL DISPLAY – 2.5% Dextrose and 0.45%)
Label for 2.5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL intravenous solution by Fresenius Kabi USA, LLC. The label includes storage instructions, manufacturer details, quantity (10 x 1000 mL single-dose flexible containers), and a barcode. Made in Germany.*

* 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.