Dextrose Injection, Solution
Product Images NDC 17271-772

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 17271-772). 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

Freeflex Logo (Dex22 0000 01)

FDA Label Image

Structural Formula (Dex22 0000 02)

Structural Formula (Dex22 0000 02)
Chemical structure of Dextrose Monohydrate, showing the molecular arrangement of the glucose ring with hydroxyl groups and one water molecule (H2O) associated, consistent with the monohydrate form.*
FDA Label Image

Figure (Dex22 0000 03)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 50 mL Bag Label)

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 50 mL Bag Label)
Label for 5% Dextrose Injection, USP, containing 2.5 grams per 50 mL (50 mg/mL) of Dextrose Monohydrate in intravenous solution form. The label includes usage instructions, storage conditions (20° to 25°C), and cautions such as single dose use and compatibility notes. It is labeled as Rx only, distributed by Becton Dickinson and Company, and manufactured by Fresenius Kabi.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 50 mL Case Label)

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 50 mL Case Label)
Label for 5% Dextrose Injection, USP, 50 mL, in a pack of 60. The label shows storage instructions at 20° to 25°C and protection from freezing. It is labeled as Freeflex by Becton Dickinson and Company, distributed by BD, and manufactured by Fresenius Kabi. The label includes lot and expiration date fields and a barcode.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 100 mL Bag Label)

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 100 mL Bag Label)
Label for 5% Dextrose Injection, USP solution, 5 grams per 100 mL, intended for intravenous use. The label includes usage instructions, storage conditions (20° to 25°C), and warnings about additives and storage. It is labeled by Becton Dickinson and Company and includes lot and expiration placeholders with barcodes.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 100 mL Case Label)

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 100 mL Case Label)
Label for 5% Dextrose Injection, USP in a 100 mL x 50 quantity package, distributed by Becton Dickinson and Company and manufactured by Fresenius Kabi. The label includes storage instructions, NDC 17271-772-03, a barcode, and contact information for product inquiries.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 50 mL Case Label)

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 50 mL Case Label)
Drug facts panel for freeflex 5% Dextrose Injection, USP, 250 mL intravenous solution. Contains 12.5 grams dextrose monohydrate per 250 mL. Includes storage instructions, usage warnings, and manufacturer information from Becton, Dickinson and Company, distributed by BD and manufactured by Fresenius Kabi.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 250 mL Case Label)

Package Label (PRINCIPAL DISPLAY – 5% Dextrose 250 mL Case Label)
Label for 5% Dextrose Injection, USP, 250 mL vials in a pack of 30, branded as freeflex by Becton Dickinson and Company. The label includes storage instructions to keep the product at 20° to 25°C (68° to 77°F) and protect from freezing. Manufactured by Fresenius Kabi, the label displays lot and expiration date fields, a barcode, and contact information for product inquiries.*

* 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.