Potassium Chloride Solution
Product Images NDC 70752-151

8 FDA label images from Quagen Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 70752-151). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quagen 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

Containerlabeling20meq473ml (Containerlabeling20meq473ml)

Containerlabeling20meq473ml (Containerlabeling20meq473ml)
Potassium Chloride Oral Solution USP, 10%, 20 mEq per 15 mL, oral solution by Quagen Pharmaceuticals LLC. The label states to dilute prior to administration and includes inactive ingredients, storage instructions, and a barcode. The container size is 473 mL. The label includes NDC 70752-150-12 and notes it is Rx only.*
FDA Label Image

Containerlabeling40meq15ml (Containerlabeling40meq15ml)

Containerlabeling40meq15ml (Containerlabeling40meq15ml)
Label for Potassium Chloride Oral Solution, USP 20%, 40 mEq per 15 mL, supplied by Quagen Pharmaceuticals LLC. The label indicates a 15 mL dose delivery, with instructions to dilute prior to administration. It specifies the product is for institutional use only and clarifies that the package is not child-resistant.*
FDA Label Image

Containerlabeling40meq473ml (Containerlabeling40meq473ml)

Containerlabeling40meq473ml (Containerlabeling40meq473ml)
Potassium Chloride Oral Solution USP 20%, 40 mEq per 15 mL, oral solution in a 473 mL bottle. The label includes dilution instructions and inactive ingredients such as citric acid and sucralose. Manufactured by Quagen Pharmaceuticals LLC, West Caldwell, NJ, with storage and safety warnings indicated.*
FDA Label Image

Cuplabeling20meq15ml (Cuplabeling20meq15ml)

Cuplabeling20meq15ml (Cuplabeling20meq15ml)
Potassium Chloride Oral Solution USP 10%, 20 mEq per 15 mL, in a single-dose container label. The label states to dilute prior to administration and includes a barcode, manufacturer information (Quagen Pharmaceuticals LLC, West Caldwell, NJ), and NDC 70752-150-02.*
FDA Label Image

Cuplabeling40meq30ml (Cuplabeling40meq30ml)

Cuplabeling40meq30ml (Cuplabeling40meq30ml)
Potassium Chloride Oral Solution, USP 10% vial label showing 40 mEq strength per 30 mL dose. The label includes dosage volume, NDC number, dilution instruction, barcode, and manufacturer Quagen Pharmaceuticals LLC, West Caldwell, NJ. It indicates the product is for institutional use only.*
FDA Label Image

Traylabel20meq15ml (Traylabel20meq15ml)

Traylabel20meq15ml (Traylabel20meq15ml)
Label for Potassium Chloride Oral Solution USP 10% showing 20 mEq per 15 mL strength. The product is manufactured by Quagen Pharmaceuticals LLC and comes in a package of 10 unit-dose cups of 15 mL. The National Drug Code (NDC) is 70752-150-48.*
FDA Label Image

Traylabel40meq15ml (Traylabel40meq15ml)

Traylabel40meq15ml (Traylabel40meq15ml)
Label for Potassium Chloride Oral Solution USP 10%, 40 mEq per 15 mL, in 10 unit-dose cups of 15 mL, manufactured by Quagen Pharmaceuticals LLC. The label includes the NDC 70752-151-48 and a barcode.*
FDA Label Image

Traylabel40meq30ml (Traylabel40meq30ml)

Traylabel40meq30ml (Traylabel40meq30ml)
Label for Potassium Chloride Oral Solution USP 10%, 40 mEq per 30 mL, manufactured by Quagen Pharmaceuticals LLC. The label includes the NDC number 70752-150-47 and indicates packaging of 10 unit-dose cups of 30 mL each. A barcode is present on the right side of the label.*

* 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.