Nicorette Lozenge
Product Images NDC 0135-0510

2 FDA label images from Haleon Us Holdings Llc · 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 Nicorette (NDC 0135-0510). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Haleon Us Holdings 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

Nicorette Lozenge Mint 2mg 144 Count Carton (104959xb Nicorette Lozenge Mint 2mg 144 Count Carton)

Nicorette Lozenge Mint 2mg 144 Count Carton (104959xb Nicorette Lozenge Mint 2mg 144 Count Carton)
Nicorette 2 mg nicotine polacrilex lozenge packaging label by Haleon US Holdings LLC. The label indicates the product is a stop smoking aid in mint flavor, containing 144 lozenges (6 containers of 24) with a dosage strength of 2 mg each. It includes a user's guide and usage information for smokers whose first cigarette is more than 30 minutes after waking.*
FDA Label Image

Nicorette Lozenge Mint 4mg 144 Count Carton (104960xb Nicorette Lozenge Mint 4mg 144 Count Carton)

Nicorette Lozenge Mint 4mg 144 Count Carton (104960xb Nicorette Lozenge Mint 4mg 144 Count Carton)
Nicorette 4 mg nicotine polacrilex lozenge packaging label. This stop smoking aid in lozenge form is mint flavored and contains 144 lozenges, divided into six POPPAC containers of 24 each. The label highlights usage instructions based on the timing of the first cigarette after waking. The product is labeled by Haleon US Holdings LLC.*

* 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.