Nicotine Polacrilex Gum, Chewing
Product Images NDC 55301-504

2 FDA label images from Aafes/your Military Exchanges · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Nicotine Polacrilex (NDC 55301-504). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aafes/your Military Exchanges, 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 Gum 2 mg And 4 mg Coated Fruit 1

Nicotine Gum 2 mg And 4 mg Coated Fruit 1
The packaging label for Exchange Select Sugar Free Nicotine Polacrilex Gum USP, 2 mg (Nicotine), a stop smoking aid. The label features the product name prominently with a note that it contains 100 pieces of gum. It includes instructions on increasing success in quitting, such as chewing at least 9 pieces per day during the first six weeks and using the gum for 12 weeks. The gum is buccal dosage form with coated fruit flavor, and the label compares it to the active ingredient in Nicorette Gum. The labeler is AAFES/Your Military Exchanges.*
FDA Label Image

Nicotine Gum 2 mg And 4 mg Coated Fruit 2

Nicotine Gum 2 mg And 4 mg Coated Fruit 2
The label is for exchange select Nicotine Polacrilex Gum USP, 4 mg (nicotine) sugar free, stop smoking aid. The package contains 100 pieces and is designed for smokers who smoke their first cigarette within 30 minutes of waking up. The label shows coated fruit flavor with actual size depiction, a 4 mg strength mark, and usage instructions to chew at least 9 pieces per day and use gum for up to 12 weeks. The labeler is AAFES/Your Military Exchanges.*

* 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.