Klor-con M Tablet, Extended Release
Product Images NDC 0245-5317

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Klor-con M (NDC 0245-5317). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, Llc, 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

Principal Display Panel (10 mEq K Tablet Bottle Label)

Label for Klor-Con M10 potassium chloride extended-release tablets USP, 750 mg, 100 count, by Upsher-Smith Laboratories, LLC. The label shows dosage strength as 10 mEq potassium, with storage and dispensing instructions, manufacturing details, and a barcode on the right.*

FDA Label Image

Principal Display Panel (15 mEq K Tablet Bottle Label)

Label for Klor-Con M15 extended-release tablets containing 1125 mg potassium chloride per tablet. The oral tablets are micro-dispersible and come in a package of 100 tablets. The label shows the manufacturer as Upsher-Smith Laboratories, LLC. It includes storage instructions, dosage note, and safety warnings such as keeping tightly closed and out of reach of children.*

FDA Label Image

Principal Display Panel (20 mEq K Tablet Bottle Label)

Label for KLOR-CON M 20 extended-release potassium chloride tablets, USP, containing 1,500 mg potassium chloride equivalent to 20 mEq potassium. The label states 100 tablets per container, Rx only, manufactured by Upsher-Smith Laboratories, LLC, with storage and dosing instructions and a barcode on the right side.*

* 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.