Potassium Chloride Solution
Product Images NDC 81033-240

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 81033-240). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kesin Pharma Corporation, 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 Label (Image0001 Cup)

Potassium Chloride Oral Solution USP, 10%, 20 mEq per 15 mL, oral solution label. The label includes instructions to dilute prior to administration, indicates unit dose delivery of 15 mL with orange flavor, and notes it is for institutional use only. Distributed by Kesin Pharma Corporation and manufactured by Saptalis Pharmaceuticals, LLC.*

FDA Label Image

20 Meq Label (Image0001)

Label for Potassium Chloride Oral Solution USP, 10%, 20 mEq/15 mL per cup, orange flavor. The label indicates it is a unit-dose oral solution with 15 mL per cup, intended for Rx use only. Manufactured by Saptalis Pharmaceuticals, LLC and distributed by Kesin Pharma Corporation. Includes storage instructions and a barcode.*

FDA Label Image

40 Meq Label (Image0002 Cup)

Label for Potassium Chloride Oral Solution USP, 10%, with a strength of 40 mEq per 30 mL. The label indicates it is an orange-flavored oral solution and instructs dilution prior to administration. It is a unit dose delivering 30 mL, labeled for institutional use only, not child resistant, and manufactured by Saptalis Pharmaceuticals, LLC, distributed by Kesin Pharma Corporation.*

FDA Label Image

40 Meq Label (Image0002)

Label for Potassium Chloride Oral Solution USP 10%, containing 40 mEq/30 mL per cup. The label states it is an orange-flavored, oral solution in unit-dose cups, each delivering 30 mL. It instructs dilution prior to administration and notes a prescription-only status. Manufactured by Saptalis Pharmaceuticals and distributed by Kesin Pharma Corporation. The label includes ingredient details, storage instructions, and warnings.*

* 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.