Potassium Chloride Injection, Solution, Concentrate
Product Images NDC 51662-1421

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 51662-1421). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Vial Label (0409 6653 18 Vial Label)

Label for Potassium Chloride Injection Concentrate, USP 40 mEq/20 mL (2 mEq/mL) in a 20 mL single-dose vial. The label highlights it is a concentrate that must be diluted before use, for intravenous administration. Distributed by Hospira, Inc., with dosage caution and bar code displayed.*

FDA Label Image

Spl Unclassified (1421 1 Spl Section)

A text panel featuring a warning indicating that the product is a concentrate and must be diluted before use. The panel contains the statement 'MUST BE DILUTED BEFORE USE' in bold uppercase letters.*

FDA Label Image

Description Chart (Description Chart 1421 1)

A data table showing concentration values of potassium chloride solution at different volumes (5 mL, 10 mL, 15 mL, 20 mL) indicating potassium ion concentration in mEq/mL, potassium chloride concentration in mg/mL, and calculated mOsmol/mL values. Each row lists additive solution size, with constant potassium ion mEq (2 mEq/mL), KCl concentration at 149 mg/mL, and osmolarity of 4 mOsmol/mL.*

FDA Label Image

Hospira (Hospira)

FDA Label Image

How Supplied (How Supplied)

A data table listing units of sale and their concentrations for an intravenous solution of Potassium Chloride, showing NDC numbers, quantities (trays of 25 single-dose containers), and corresponding concentrations in mEq and mL.*

FDA Label Image

Serialized Label (Serialized Potassium Chloride)

Potassium chloride injection concentrate 40 mEq/20 mL (2 mEq/mL) in a 20 mL single-dose vial for intravenous use. The vial has a black cap and a label indicating that the product must be diluted before use. Distributed by HF Acquisition Co LLC, DBA HealthFirst.*

* 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.