Nicotine Transdermal System Film, Extended Release
Product Images NDC 76282-783

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nicotine Transdermal System (NDC 76282-783). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Exelan Pharmaceuticals, 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

Step 1 (Step 1)

Clear Nicotine Transdermal System Patch 21 mg/24h extended release film by Exelan Pharmaceuticals, Inc. Front and side panels show product name, strength, stop smoking aid indication, step 1 usage instructions, and warnings. Includes behavior support program with self-help guide. Contains 14 patches, delivered transdermally over 24 hours.*

FDA Label Image

Step 2 (Step 2)

Packaging label for Clear Nicotine Transdermal System Patch 14 mg delivered over 24 hours, an extended-release film for transdermal use. The label highlights the product as a stop smoking aid, includes directions for use, safety warnings, and a behavioral support program with a self-help guide. Manufactured for Exelan Pharmaceuticals, Inc., the package contains 14 patches with clear usage instructions based on cigarette consumption.*

FDA Label Image

Step 3 (Step 3)

The packaging label for Clear Nicotine Transdermal System Patch, 7 mg delivered over 24 hours, an extended-release transdermal film used as a stop smoking aid. It includes directions for use, warnings, and a chart for patch strength based on cigarettes smoked daily. Manufactured by Aveva Drug Delivery Systems and distributed by Exelan Pharmaceuticals, Inc., Boca Raton, FL. The package contains 14 patches and includes behavior support program information.*

* 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.