Dr. Scholls Blister Pain Relief Complete Kit
Product Images NDC 73469-0488

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dr. Scholls Blister Pain Relief Complete (NDC 73469-0488). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Scholl's Wellness Company 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

Inner Package (Inner Package)

Inner Package (Inner Package)
The image displays multiple identical Drug Facts panels for Dr. Scholls 4% Lidocaine Patch, an external analgesic. It includes active ingredient information, uses, warnings, directions for adults and children over 12, inactive ingredients, storage instructions, and contact information for questions. The panels also mention precautions for pregnant or breastfeeding individuals and advice to stop use and consult a doctor if conditions worsen.*
FDA Label Image

Outer Package (Outer Package)

Outer Package (Outer Package)
Dr. Scholl's Blister Pain Relief Complete Kit packaging label features LIDOCAINE 4% indicated for seal and heal bandages. The front highlights 12 lidocaine patches and 12 hydrogel bandages for clinically tested 12-hour pain relief. The label includes instructions for use, active and inactive ingredients, warnings, and directions. Distributed by Scholl's Wellness Company LLC.*
FDA Label Image

Box (Box)

Box (Box)
Dr. Scholls Blister Pain Relief Complete kit label showing a white background with repeated blue Dr. Scholl's logos arranged in rows. The lot number S269A is printed at the bottom center of the label. No additional product details or usage information are visible.*

* 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.