Good Sense Nicotine
Product Images NDC 68258-7992

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Good Sense Nicotine (NDC 68258-7992). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, Inc., 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

Ndc 68258-7992-07 (Ndc 68258 7992 07 Perrigo)

good sense nicotine Polacrilex 4 mg lozenges label by Dispensing Solutions, Inc. The label shows 72 lozenges with active ingredient nicotine polacrilex 4 mg per lozenge, mint flavor. It includes usage directions, NDC 68258-7992-07, and states purpose as smoking cessation aid. The label features batch and sample lot information, storage instructions, and the DispenseQuick logo.*

FDA Label Image

Smoke Free Habits.com Image (Ee345181 4999 4948 9589 7d70d61885ad 01)

FDA Label Image

Step 1 Image (Ee345181 4999 4948 9589 7d70d61885ad 02)

Instructional step label reading 'STEP 1 1 lozenge every 1 to 2 hours' in white text on a red rectangular background. This panel provides dosage frequency guidance for good sense nicotine lozenges.*

FDA Label Image

Step 2 Image (Ee345181 4999 4948 9589 7d70d61885ad 03)

Instructional graphic showing Step 2 dosing direction for Good Sense Nicotine lozenge, stating to take 1 lozenge every 2 to 4 hours. The design features white text on a blue rounded square background, indicating a stepwise usage guideline.*

FDA Label Image

Step 3 Image (Ee345181 4999 4948 9589 7d70d61885ad 04)

Instructional label showing dosing directions as Step 3: take 1 lozenge every 4 to 8 hours.*

FDA Label Image

12 Weeks After Quit Date Image (Ee345181 4999 4948 9589 7d70d61885ad 05)

* 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.