Nicotine Patch, Extended Release
Product Images NDC 11673-196

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nicotine (NDC 11673-196). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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 Target 14 mg 14 Count Carton (Nicotine Patch Target 14 mg 14 Count Carton)

The label depicts the up&up nicotine patch 14 mg/24h transdermal system, a stop smoking aid patch. This package contains 14 clear patches representing a 2-week kit and is identified as Step 2. The label highlights dosing guidance based on cigarettes smoked per day and notes comparison to the active ingredient in NicoDerm CQ. The labeler is Target Corporation.*

FDA Label Image

Nicotine Patch Target 7 mg 14 Count Carton (Nicotine Patch Target 7 mg 14 Count Carton)

The packaging label for the up&up nicotine patch displays a 7 mg/24h nicotine transdermal system intended as a stop smoking aid. The label indicates this is step 3 of the program and contains 14 clear patches, representing a two-week kit, from Target Corporation. The package highlights comparison to NicoDerm CQ active ingredient.*

FDA Label Image

Nicotine Patch Target 21 mg 14 Count Carton (Image 01)

Packaging label of up&up Nicotine Patch 21 mg/24h extended-release transdermal system. The box contains 14 clear patches intended as a 2-week kit. The label highlights its use as a stop smoking aid and compares to the active ingredient in NicoDerm CQ. Step 1 is indicated for smokers of more than 10 cigarettes per day.*

* 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.