Potassium Chloride
Product Images NDC 14789-136

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 14789-136). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nexus Pharmaceuticals 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

Principal Display Panel – 10 mL Carton Label (Pot0w 0004 01)

Potassium Chloride Injection Concentrate USP 20 mEq/10 mL (2 mEq/mL) vial label by Nexus Pharmaceuticals LLC. The packaging is for 25 single-dose 10 mL vials. The label indicates that this is a concentrate requiring dilution before use, intended for intravenous administration only. It includes storage and aseptic technique instructions, product concentration details, and manufacturer information.*

FDA Label Image

Principal Display Panel – 10 mL Vial Label (Pot0w 0004 02)

Potassium Chloride For Injection Concentrate, USP 20 mEq/10 mL (2 mEq/mL) single-dose vial label from Nexus Pharmaceuticals LLC. The label includes dilution warning and usage instructions, noting it is for intravenous use only. The label also lists potassium chloride content and additional product details.*

FDA Label Image

Principal Display Panel – 20 mL Carton Label (Pot0w 0004 03)

Potassium Chloride Concentrate for Injection, USP 40 mEq/20 mL (2 mEq/mL) in single-dose vials. The label indicates it is a concentrate requiring dilution before use, manufactured by Nexus Pharmaceuticals LLC. The package contains 25 vials of 20 mL each, intended for intravenous use and sterile, nonpyrogenic solution.*

FDA Label Image

Principal Display Panel – 20 mL Vial Label (Pot0w 0004 04)

Potassium Chloride for Injection Concentrate USP 40 mEq/20 mL (2 mEq/mL) vial label. The label indicates the product is a single-dose vial for intravenous use, with a warning that the concentrate must be diluted before use. It is manufactured by Nexus Pharmaceuticals LLC, Lincolnshire, IL, USA. The label includes dosage information and a barcode.*

* 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.