Potassium Chloride Solution
Product Images NDC 27808-169

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 27808-169). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tris Pharma 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

10% Label (Potassium Chloride Oral Solution 1)

Potassium Chloride Oral Solution USP 10%, 20 mEq per 15 mL, in a 16 oz (473 mL) bottle label. The label states to dilute prior to administration and that the product is Rx only. It includes inactive ingredients, storage instructions, and manufacturer information for Tris Pharma Inc., Monmouth Junction, NJ.*

FDA Label Image

20% Label (Potassium Chloride Oral Solution 2)

Potassium Chloride Oral Solution, USP 20%, containing 40 mEq per 15 mL, in a 16 oz (473 mL) bottle. The label advises dilution prior to administration and lists inactive ingredients such as Citric Acid Anhydrous and FD&C Yellow 6. Manufactured by Tris Pharma Inc, Monmouth Junction, NJ. Includes storage instructions and 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.