Mybiooid Lidocaine 4% Pain Relieving Gel-patch
Product Images NDC 88068-001

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mybiooid Lidocaine 4% Pain Relieving Gel-patch (NDC 88068-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avelon Trading Limited, 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

1 (15patch)

The packaging label for Mybiooid Lidocaine 4% Pain Relieving Gel-Patch features a green and white color scheme with a central image of a patch applied on the lower back of a human figure. The product is highlighted as providing odor-free, targeted numbing relief, and staying in place with an extra-secure cover, lasting up to 8 hours. The label indicates the package contains 15 patches, measuring 5.5 by 3.94 inches, suitable for application on neck, shoulder, back, and wrist. Additional sections of the label show drug facts, directions for use, warnings, active and inactive ingredients, manufacturer information, and illustrated application instructions. The labeler is Avelon Trading Limited.*

FDA Label Image

2 (33patch)

Mybiooid Lidocaine 4% Pain Relieving Gel-Patch packaging label, displaying a green and white box with red and yellow accents. The front highlights the product's name, 4% lidocaine strength, and features an image showing patch application on a person's back. It mentions features like odor-free, targeted numbing relief, and extra-secure cover lasting up to 8 hours. The package contains 33 patches (5.5" x 3.94") and illustrates use for neck, shoulder, back, and wrist. The label also includes directions, warnings, drug facts, and manufacturer information for Avelon Trading Limited.*

* 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.