Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 17271-735

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 17271-735). 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 (Dex20 0000 01)

FDA Label Image

Structural Formula (Dex20 0000 02)

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Logo (Dex20 0000 03)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 500 mL Bag Label)

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 500 mL Bag Label)
This text contains important information about a pharmaceutical product called freeflex® NDC 17271-735-06, which is a 500 mL solution containing 5% Dextrose and 0.9% Sodium Chloride for intravenous use. It provides details about the composition, electrolyte levels, storage instructions, and precautions for use. The product is a single-dose container that must be used immediately after removal from the overwrap. It is sterile, non-PVC, and non-DEHP. The text also includes details about the manufacturer, Becton, Dickinson and Company, and contact information for product inquiries.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 500 mL Shipper Label)

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 500 mL Shipper Label)
This text provides details about a medication product with the NDC code 17271-735-06, containing 5% Dextrose and 0.9% Sodium Chloride in a 500mL x 20 injection, to be stored at a temperature range of 20° to 25°C. The product is distributed by BD and manufactured by Fresenius Kabi. Contact information for product inquiries is included as well.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 1,000 mL Bag Label)

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 1,000 mL Bag Label)
This is a description of a medical product called "freeflex® 1000 mL", which is a 5% Dextrose and 0.9% Sodium Chloride Injection intended for intravenous use. Each 100 mL contains Dextrose and Sodium Chloride in specific amounts. The electrolyte content per 1000 mL is specified. It is advised that additives may be incompatible and to consult with a pharmacist when necessary. The usual dosage information and storage conditions are provided. The product is packaged in a single-dose container with a moisture barrier overwrap, and the closure is latex-free. The manufacturer and contact information are listed as well.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 1000 mL Shipper Label)

Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 1000 mL Shipper Label)
This text provides information about an intravenous solution containing 5% Dextrose and 0.9% Sodium Chloride in a 1,000 mL pack. The product should be stored at a temperature between 20° to 25°C (68° to 77°F), protected from freezing. The manufacturer is Becton, Dickinson and Company, with product inquiry contact number as 1-800-523-0502. The product is distributed by BD and manufactured by Fresenius Kabi.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.