Potassium Chloride Injection, Solution
Product Images NDC 63323-669

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 63323-669). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structural Formula (Pot0c 0002 01)

Chemical structure of Dextrose Monohydrate, shown as part of the combined active ingredients for Potassium Chloride Injection, Solution by Fresenius Kabi USA, LLC.*

FDA Label Image

Fresenius Kabi Logo (Pot0c 0002 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 10 mEq/L Bag Label)

Potassium Chloride 10 mEq/100 mL Injection, USP in 5% Dextrose solution. The label indicates the solution contains 75 mg Potassium Chloride and 5 g Dextrose Hydrous per 100 mL. This single-dose intravenous injection is supplied in a 1000 mL container by Fresenius Kabi USA, LLC, made in Norway, with storage instructions and usage warnings included.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 10 mEq/L Shipper Label)

Label for Potassium Chloride in 5% Dextrose Injection, USP, 10 mEq strength, in a 1000 mL vial with 10 vials per package. The injection solution is manufactured by Fresenius Kabi USA, LLC, made in Norway. Storage instructions specify 20° to 25°C (68° to 77°F) with avoidance of excessive heat. The label includes barcodes, lot number, expiry date placeholder, and quantity information.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 20 mEq/L Bag Label)

Label for Potassium Chloride 20 mEq Injection in 5% Dextrose, USP, 1000 mL solution for intravenous use. Each 100 mL contains 5 g Dextrose Hydrous and 150 mg Potassium Chloride. Electrolyte concentrations per 1000 mL are potassium 20 mEq and chloride 20 mEq. Manufactured by Fresenius Kabi USA, LLC, made in Norway.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 20 mEq/L Shipper Label)

Label for Potassium Chloride 20 mEq in 5% Dextrose Injection, USP, 1000 mL, package of 10. The label includes storage instructions, manufacturer information (Fresenius Kabi USA, LLC), and barcodes. It indicates the product is made in Norway and is for intravenous use.*

* 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.