Biofreeze Gel
Product Images NDC 59316-101

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Biofreeze (NDC 59316-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Reckitt Benckiser 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

Biofreeze 01

Drug Facts panel of Biofreeze Pain Relieving Roll-On, displaying active ingredient Menthol USP 3.5% as a cooling pain reliever. The text details uses, warnings, directions, and inactive ingredients. It includes instructions for application, safety information, and a customer service phone number. The label emphasizes cryotherapy as the cold method and indicates no animal testing.*

FDA Label Image

Biofreeze 02

Label for Biofreeze Pain Relieving Gel containing 35 mg/mL menthol, manufactured by Performance Health Inc. The label highlights its use for arthritis, sore muscles, and joint back pain. The package size is 16 fl oz (473 mL). The label features usage instructions, warnings, inactive ingredients, and contact information, with a note that it is manufactured in the USA with no animal testing.*

* 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.