Quitine Mini Nicotine Lozenge
Product Images NDC 84720-009

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quitine Mini Nicotine (NDC 84720-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quitine 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

957-qe-mini-nicotine-lozenges.jpg (957 Qe Mini Nicotine Lozenges)

Quitine Mini Nicotine Lozenges 4 mg mint flavored, oral lozenges containing Nicotine Polacrilex for stop smoking aid. The light blue carton shows 216 mini lozenges in 8 mini QuitTube containers of 27 each. The labeler is Quitine LLC, Lewes, Delaware, with NDC 84720-009-07. Packaging includes Drug Facts, directions, tamper-evident feature, and a QR code for promotional scanning.*

FDA Label Image

Calendar-reminders-image-one.jpg (Calendar Reminders Image One)

An instructional diagram showing a four-step reminder schedule for using lozenges. Steps indicate specific lozenge dosing intervals at various weeks: Step 1 at weeks 1 with 1 lozenge every 1 to 2 hours, Step 2 at week 7 dosing every 2 to 4 hours, Step 3 at week 10 dosing every 4 to 8 hours, and a final step labeled EX-SMOKER at 12 weeks after the quit date.*

FDA Label Image

Free-personalized-plan-image-two.jpg (Image 01)

FDA Label Image

Wallet-card-image-three.jpg (Image 02)

An informational wallet card illustration for quitine mini nicotine lozenge users. The card has two sections: the first provides space for writing personal reasons to quit smoking, and the second lists contact numbers for the American Lung Association, American Cancer Society, American Heart Association, and prompts to contact a quitting buddy or friend.*

* 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.