Nicotine Patch, Extended Release
Product Images NDC 70677-1265

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nicotine (NDC 70677-1265). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strategic Sourcing Services 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

Carton (Mckesson Nicotine Patch 14 mg)

Nicotine Transdermal System Patch Step 2, 14 mg/24 hours, extended release patch for transdermal use. The packaging shows a 14-patch supply labeled as a stop smoking aid, including a behavior support program with a self-help guide. Manufactured by Strategic Sourcing Services LLC and distributed by McKesson Corp. The label includes drug facts, warnings, directions, and inactive ingredients.*

FDA Label Image

Carton (Mckesson Nicotine Patch 21 mg)

Foster & Thrive Nicotine Transdermal System Patch Step 1, 21 mg delivered over 24 hours, extended release patch for stop smoking aid. The carton contains 28 patches (4-week kit) and is labeled for use in a stepwise quitting program. Labeler is Strategic Sourcing Services LLC. The packaging includes detailed drug facts, warnings, usage directions, and customer support information.*

FDA Label Image

Carton (Mckesson Nicotine Patch 7 mg)

Packaging label for Foster & Thrive Nicotine Transdermal System Patch Step 3 delivering 7 mg of nicotine over 24 hours. This stop smoking aid comes in a 14-patch (2 week kit) extended-release patch form. The label includes usage directions, warnings, inactive ingredients, and customer support contact information. It is labeled for use after completing Step 2 and includes a behavior support program with a self-help guide.*

* 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.