Dextrose In Lactated Ringers Injection, Solution
Product Images NDC 0264-7751

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dextrose In Lactated Ringers (NDC 0264-7751). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by B. Braun Medical Inc., 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

Chemical Structure (Dextrose In Lactated Ringers Injection Usp In Exce 1)

Chemical structure diagram of the active ingredient dextrose, showing its molecular configuration, including hydroxyl groups and a ring structure, as part of the Dextrose in Lactated Ringers injection solution by B. Braun Medical Inc.*

FDA Label Image

Recycle Symbol (Dextrose In Lactated Ringers Injection Usp In Exce 2)

FDA Label Image

1000 mL Container Label L7510 (Dextrose In Lactated Ringers Injection Usp In Exce 3)

Label for Dextrose in Lactated Ringer's Injection, 5% dextrose concentration, in a 1000 mL Excel container by B. Braun Medical Inc. The label lists active ingredients including hydrous dextrose, sodium chloride, sodium lactate, potassium chloride, and calcium chloride with corresponding strengths per 100 mL. Additional details include pH, osmolarity, electrolytes, warnings, storage instructions, and manufacturer information in Bethlehem, PA.*

FDA Label Image

Recycle Symbol (Dextrose In Lactated Ringers Injection Usp In Exce 4)

FDA Label Image

500 mL Container Label L7511 (Dextrose In Lactated Ringers Injection Usp In Exce 5)

Label for 5% Dextrose in Lactated Ringer's Injection, 500 mL solution for intravenous use. The label lists active ingredients with their respective concentrations per 100 mL: Dextrose 5 g, Sodium Chloride 0.6 g, Sodium Lactate 0.31 g, Potassium Chloride 0.03 g, Calcium Chloride 0.02 g, and water for injection. It states the product is sterile and nonpyrogenic, for single-dose use only, includes warnings, storage instructions, and the manufacturer as B. Braun Medical Inc. The NDC number is 0264-7751-10.*

* 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.