Potassium Chloride Solution
Product Images NDC 50268-674

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 50268-674). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

50 (674 15)

Label for Potassium Chloride Oral Solution USP, 10%, containing 20 mEq per 15 mL, supplied as a 50-unit pack of 15 mL each. The label includes warnings to dilute prior to administration and shake well to avoid freezing, specifies it is for prescription use only, and indicates the product is orange flavored. It is manufactured by AvPAK, with storage instructions and a list of inactive ingredients provided.*

FDA Label Image

1 (675 12)

Potassium Chloride Oral Solution USP, 20% label showing 40 mEq per 15 mL strength. The label includes instructions to dilute prior to administration, shake well, and avoid freezing. It indicates a 15 mL delivery volume with orange flavor, and is marked Rx only. Manufactured for AvPAK in Pulaski, TN, the label provides storage and handling details along with a barcode.*

* 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.