Dr. Scholls Blister Pain Relief Complete Kit
Product Images NDC 73469-0487

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 73469-0487). 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 Label (Inner Package)

This image shows multiple instances of drug facts panels for Dr. Scholls 4% Lidocaine Patch, an external analgesic. The panels include the active ingredient (Lidocaine 4%), usage directions, warnings for external use only, storage information, inactive ingredients, and contact information for questions. Directions specify use for adults and children over 12 years, with advice to consult a doctor for younger children.*

FDA Label Image

Box (Box)

Back label of Dr. Scholls Blister Pain Relief Complete kit showing multiple repetitions of the Dr. Scholls oval logo in blue on a white background. A lot number (S269A) is printed at the bottom center inside a blue-bordered box. No additional product information or text is visible.*

FDA Label Image

Label (Label)

Dr. Scholls Blister Pain Relief Complete Kit packaging label prominently features the Dr. Scholl's logo with a yellow and red color scheme. The product contains lidocaine 4% as the active ingredient and includes 8 lidocaine patches and 8 hydrogel bandages. The label highlights clinically tested 12-hour pain relief for blisters and provides detailed instructions for use, warnings, and drug facts. The labeler is Scholl's Wellness Company 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.