Potassium Chloride Injection, Solution, Concentrate
Product Images NDC 0404-9936

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 0404-9936). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

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A data table listing product codes, units of sale, total potassium ion content, potassium chloride per mL, and associated NDCs for Potassium Chloride injection solution vials. It includes information on vial volumes of 5 mL, 10 mL, and 20 mL single dose vials with varying potassium ion amounts.*

FDA Label Image

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A data table presenting information on Potassium Chloride injection concentrate with total potassium ion content and packaging details. It includes product code 96730, NDC 63323-967-30 sold as a unit of 25, containing 60 mEq (2.35 g) total potassium ion and 149 mg potassium chloride per mL. The individual unit is a 30 mL multiple dose vial labeled NDC 63323-967-01.*

FDA Label Image

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Potassium Chloride 2 mEq/mL Injection Concentrate, USP, single dose vial label showing 40 mEq per 20 mL strength. The label indicates intravenous use, dilution requirement prior to administration, and that the product is sterile, nonpyrogenic, free of natural rubber latex and preservatives. It includes storage instructions, NDC 0404-9936-20, and is packaged by Henry Schein, Inc., Bastian, VA.*

FDA Label Image

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Label for Potassium Chloride 10 mEq/5 mL injection concentrate, USP, single dose vial. The concentrate has a strength of 2 mEq/mL in a 5 mL vial. It is preservative-free, sterile, nonpyrogenic, and requires dilution before intravenous administration. The label notes the vial stopper does not contain natural rubber latex. Packaged by Henry Schein, Inc., with storage instructions at controlled room temperature 68°F to 77°F. Contains barcodes and lot/expiration placeholders.*

* 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.