Potassium Chloride Injection, Solution, Concentrate
Product Images NDC 51662-1387

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 51662-1387). 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

Description (Description)

A data table showing additive solution concentrations and sizes for Potassium Chloride injection, solution, concentrate at 149 mg/mL. The table lists K+ mEq/mL, KCl mg/mL (149), and calculated mOsmol/mL (4) for varying additive solution sizes from 10 mEq/5 mL to 40 mEq/20 mL.*

FDA Label Image

Logo (How Supplied Logo)

FDA Label Image

How Supplied (How Supplied)

A data table listing units of sale and concentrations for potassium chloride injection, solution, concentrate. It details various NDCs with trays of 25 single-dose containers and corresponding concentrations ranging from 10 mEq/5 mL to 40 mEq/20 mL at 2 mEq/mL.*

FDA Label Image

Serialized Labeling (Serialized Vial Labeling)

Close-up image of a medication vial with a black cap showing the label for Potassium Chloride injection concentrate. The label states the strength as 20 mEq/10 mL (2 mEq/mL) and includes a warning that it must be diluted before use. The vial is distributed by HF Acquisition Co LLC, Mukilteo, WA, with visible lot and barcode information.*

FDA Label Image

Spl Table (Spl Unclassified)

A text panel featuring two lines: the word 'CONCENTRATE' in a blue shaded box above a beige shaded box with the text 'MUST BE DILUTED BEFORE USE.' This label indicates the concentrated nature of the medication requiring dilution prior to administration.*

FDA Label Image

Vial Labeling (Vial Labeling)

Label for Potassium Chloride Injection Concentrate USP, 20 mEq/10 mL (2 mEq/mL) in a 10 mL single-dose vial. The label states it must be diluted before use and is for intravenous administration, Rx only. Distributed by Hospira, Inc., Lake Forest, IL. Contains potassium chloride 2 mEq (149 mg) per mL, sterile, nonpyrogenic, with pH adjustment possible with HCl.*

* 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.