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Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 63323-873
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 63323-873). 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.
Structural Formula (Dex1c 0000 02)
Chemical structure of Dextrose Monohydrate, showing the glucose ring with hydroxyl groups and a water molecule (H2O) associated.*
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Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 250 mL Bag Label)
Label for Dextrose and Sodium Chloride Injection, USP, 5% Dextrose and 0.225% Sodium Chloride in 250 mL intravenous solution by Fresenius Kabi USA, LLC. The label includes contents per 100 mL, usage instructions, storage conditions (20° to 25°C), and container closure details. Product made in Germany, with barcode and lot/expiration placeholders.*
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 500 mL Bag Label)
Label for Dextrose and Sodium Chloride Injection, USP, 5% Dextrose and 0.225% Sodium Chloride, 500 mL intravenous solution. Manufactured by Fresenius Kabi USA, LLC, made in Germany. The label includes content details, storage instructions, and barcode.*
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 1000 mL Bag Label)
Label for 5% Dextrose and 0.225% Sodium Chloride Injection, USP, 1000 mL intravenous solution by Fresenius Kabi USA, LLC. The label details active ingredient amounts per 100 mL, storage instructions, and usage precautions. The product is single-dose, sterile, and 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.
