Potassium Chloride
Product Images NDC 60505-6185

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 60505-6185). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp, 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

Btl10

Potassium Chloride Oral Solution USP, 10% (20 mEq per 15 mL) label from Apotex Corp featuring a 473 mL bottle size. The label includes dosing instructions to dilute prior to administration, inactive ingredients list, storage conditions, and safety warnings. It also shows NDC 60505-6184-6 and manufacturer information for Apotex Inc. Canada and Apotex Corp. Florida.*

FDA Label Image

Btl20

Label for Potassium Chloride Oral Solution USP, 20% (40 mEq per 15 mL), a 473 mL liquid solution by Apotex Corp. The label includes usage instructions to dilute prior to administration, a barcode, and storage information. Manufactured by Apotex Inc., Toronto, Canada, and for Apotex Corp., Weston, Florida.*

FDA Label Image

Crt10

Potassium Chloride Oral Solution USP, 10% (20 mEq per 15 mL), in a 473 mL volume size, manufactured by Apotex Corp. The label instructs "Dilute prior to administration" and states Rx only. The packaging includes storage and inactive ingredient information, dosage instructions, and manufacturer details with barcode and NDC 60505-6184-6.*

FDA Label Image

Crt20

Potassium Chloride Oral Solution USP, 20%, containing 40 mEq per 15 mL, in a 473 mL bottle. The label shows active ingredient concentration, inactive ingredients, storage instructions (20°C to 25°C), and manufacturer Apotex Corp. The text advises to dilute prior to administration and states it is Rx only.*

* 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.