Potassium Chloride Solution
Product Images NDC 59651-959

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 59651-959). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (20 mEq per 15 mL (473 mL Bottle Label))

Label for Potassium Chloride Oral Solution USP, 10%, 20 mEq per 15 mL, oral solution by Aurobindo Pharma Limited. The label states dilution prior to administration, volume of 473 mL, inactive ingredients, storage conditions, and distributor information for Aurobindo Pharma USA, Inc., East Windsor, NJ. It includes a barcode and mentions packaging details.*

FDA Label Image

Package Label-principal Display Panel (40 mEq per 15 mL (473 mL Bottle Label))

Label for Potassium Chloride Oral Solution USP 20%, 40 mEq per 15 mL, a human prescription drug solution for oral use. The label includes the instruction to dilute prior to administration, lists inactive ingredients, storage instructions, and distributor information for Aurobindo Pharma USA, Inc. The container size is 473 mL and it is made in India by Aurobindo Pharma Limited.*

* 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.