Potassium Chloride Solution
Product Images NDC 31722-495

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 31722-495). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, 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

20 Meq (20meq Cl Counts)

Text panel listing inactive ingredients for Potassium Chloride oral solution including citric acid anhydrous, FD&C Yellow#6, glycerin, methylparaben, and others. It states that each 15 mL tablespoon contains 20 mEq of potassium chloride. The labeler Camber Pharmaceuticals, Inc. is visible on the adjoining panel.*

FDA Label Image

40 Meq (40meq Cl Counts)

Potassium Chloride Oral Solution, USP 20%, 40 mEq per 15 mL, by Camber Pharmaceuticals, Inc. The label indicates a 473 mL bottle intended for prescription use only. It includes a warning to dilute prior to administration and storage instructions. The back label lists inactive ingredients and manufacturer details, noting it is manufactured by Ascent Pharmaceuticals, Inc. for Camber Pharmaceuticals.*

* 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.