Hot/cold Medicated Patch
Product Images NDC 67777-201

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hot/cold Medicated Patch (NDC 67777-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dynarex, 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

1450_bx_master (1450 Bx Master R241011 2)

The packaging label for Hot/Cold Medicated Patches by Dynarex displays 'COLD HOT Medicated Patches X-Large Back' prominently with the We Care logo. It includes directions, warnings, active ingredient menthol 5%, and product quantity of 3 patches (5.5" x 9.8"). The label features an image of a person applying a patch to their lower back and instructions for topical use.*

FDA Label Image

1451_in_master (1451 In Master R241114 2)

Packaging label for We Care Cold Hot Medicated Patches, topical patches for arm and neck pain relief. The label shows the product name prominently in blue and red, indicating cold and hot effect. The box includes drug facts with menthol 5% as the active ingredient and is manufactured for Dynarex Corporation. The package contains 5 patches, each measuring 3.2 by 4.7 inches, and highlights key benefits like immediate pain relief and long-lasting effect up to 8 hours. The label displays item number 1451 and branding elements from We Care and Dynarex.*

FDA Label Image

1452_in_master (1452 In Master R241114 2)

Packaging label for Hot/Cold Medicated Patch by Dynarex, showing the product name in blue and red text, and a photo of a person applying the patch to their lower back. The label highlights natural menthol 5%, and lists features such as immediate pain relief and long-lasting effect. The label includes the Drug Facts section and directions, the manufacturer information, and the product NDC 67777-201.*

* 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.