Nicotine Patch, Extended Release
Product Images NDC 59450-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nicotine (NDC 59450-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Kroger Co., 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

Nicotine Patch 14 mg (Nicotine Patch 14 mg)

Packaging label for Nicotine Transdermal System Patch 14 mg Step 2 by The Kroger Co. The label indicates it is a 14 mg/24h extended release patch used as a stop smoking aid. The box contains 14 patches and highlights a behavior support program with a self-help guide. The label includes drug facts, directions, warnings, and manufacturer details.*

FDA Label Image

Nicotine Patch 21mg (Nicotine Patch 21mg)

Nicotine transdermal system patch 21 mg Step 1 by The Kroger Co. is an extended-release transdermal patch for smoking cessation support. The package contains 14 patches, delivering nicotine over 24 hours. The label includes usage directions, warnings, and information about the included behavior support program with a self-help guide. The pack is branded with Kroger quality guarantee and pharmacist recommendation statements.*

FDA Label Image

Nicotine Patch 7 mg (Nicotine Patch 7 mg)

Packaging label for Kroger Nicotine Transdermal System Patch Step 3, 7 mg delivered over 24 hours, an extended release transdermal patch used as a stop smoking aid. The box contains 14 patches and includes information about the behavior support program with a self-help guide. The label highlights this is step 3 in a three-step system and emphasizes usage after completing step 2.*

* 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.