Potassium Chloride In Dextrose Injection, Solution
Product Images NDC 0338-0683

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride In Dextrose (NDC 0338-0683). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare 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

Chemical Structure (Image 01)

Chemical structure of D-Glucose monohydrate, depicting its molecular arrangement including hydroxyl groups and hydration with one water molecule.*

FDA Label Image

Potassium Chloride In Dextrose Representative Carton Label 0338-0683-04 (Image 02)

This image displays a text label describing printing details for a Baxter Healthcare intravenous injection solution. It specifies a 20 mEq Potassium Chloride in 5% Dextrose USP solution in a 1000 mL VIAFLEX Plus container. It includes placeholders for expiration date, lot number, primary and secondary barcodes, and notes on date formatting and barcode encoding.*

FDA Label Image

Potassium Chloride In Dextrose Representative Container Label Ndc 0338-0683-04 (Image 03)

Label for Potassium Chloride Injection, 20 mEq in 5% Dextrose Injection USP, 1000 mL solution by Baxter Healthcare Company. The label states 5 g Dextrose Hydrous, 150 mg Potassium Chloride per 100 mL. Includes dosage and storage instructions, Lot, Expiration, and NDC 0338-0683-04. Contains proprietary and manufacturer information for Baxter Healthcare.*

* 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.