Dextrose Injection, Solution
Product Images NDC 17271-720

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 17271-720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Becton Dickinson And Company, 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

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The image shows a multiple-dose vial labeled Dextrose Injection, USP with a strength of 50 mg/mL. It is a clear solution intended for intravenous use, supplied by Becton Dickinson and Company. The vial features a blue and white label with the proprietary name Dextrose prominently displayed.*
FDA Label Image

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Chemical structure of Dextrose Monohydrate depicting a cyclic sugar molecule with multiple hydroxyl groups and a water molecule (H2O) attached, representing the hydrated form of Dextrose.*
FDA Label Image

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FDA Label Image

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Label for 5% Dextrose Injection, USP, showing strength of 2.5 grams per 50 mL (50 mg per mL) for intravenous use. The label includes detailed content information, such as Dextrose monohydrate quantity per 100 mL and storage instructions. It is distributed by Becton Dickinson and Company and manufactured by Fresenius Kabi in Norway. The label includes barcode and regulatory information.*
FDA Label Image

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Label for 5% Dextrose Injection, USP, 50 mL x 60 vials, an intravenous solution by Becton Dickinson and Company. The label includes storage instructions (20° to 25°C, protect from freezing), manufacturer information (Fresenius Kabi, Norway), and barcodes along with spaces for expiration date and lot number.*

* 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.