Sterile Water Injection, Solution
Product Images NDC 17271-750

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sterile Water (NDC 17271-750). 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

Free Flex Logo (Bdx0j 0000 01)

Sterile Water 1000 mL intravenous injection solution by Becton Dickinson and Company. The image shows the front label of a clear plastic bag with the proprietary name 'Sterile Water' prominently displayed. The label indicates it is a 1000 mL volume and intended for intravenous use. The Becton Dickinson logo is visible on the label.*

FDA Label Image

Becton, Dickinson And Company Logo (Bdx0j 0000 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Sterile Water for Injection Bag Label)

Label for freeflex Sterile Water for Injection, USP 1000 mL intravenous injection solution. The label includes warnings about non-isotonic properties and usage restrictions, manufacturer information showing Becton, Dickinson and Company as labeler and Fresenius Kabi as manufacturer, and storage instructions. The product is a single-dose container designed for drug diluent use only and specifies that it is not made with natural rubber latex.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Sterile Water for Injection Case Label)

Label for Sterile Water for Injection, USP, 1000 mL, packaged in a set of 10. The label includes storage instructions (20° to 25°C, protect from freezing), and identifies Becton, Dickinson and Company as the distributor and Fresenius Kabi as the manufacturer. The product NDC is 17271-750-07.*

* 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.