Potassium Chloride Injection, Solution, Concentrate
Product Images NDC 0404-9937

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 0404-9937). 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 text panel with a warning for Potassium Chloride Injection, Solution, Concentrate stating "CONCENTRATE" and "MUST BE DILUTED BEFORE USE." This emphasizes the importance of dilution before administration.*

FDA Label Image

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Data table showing concentrations of potassium (K+) and potassium chloride (KCl) in various additive solution sizes of Potassium Chloride injection concentrate. For solution sizes from 5 mL to 20 mL, K+ is consistently 2 mEq/mL, KCl is 149 mg/mL, and calculated osmolarity is 4 mOsmol/mL. A note mentions possible hydrochloric acid for pH adjustment.*

FDA Label Image

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Data table presenting unit of sale and concentration information for Potassium Chloride injection solutions. It lists NDC codes, package size as trays of 25 single-dose containers, and concentrations in mEq per mL and mL volumes, ranging from 10 to 40 mEq per container with a concentration of 2 mEq/mL.*

FDA Label Image

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Potassium Chloride 20 mEq/10 mL injection concentrate, USP, single dose vial label. The label indicates a concentration of 2 mEq/mL in 10 mL volume for intravenous use only, requiring dilution before use. Packaged by Henry Schein, Inc., with storage instructions and barcode visible. The label includes manufacturer and lot information areas with 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.