Biofreeze Overnight Roll-on Gel
Product Images NDC 59316-207

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Biofreeze Overnight Roll-on (NDC 59316-207). 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

Back Label (59316 209 Back Label)

Drug Facts panels for Biofreeze Overnight Relief Roll-On and Biofreeze Roll-On topical gels containing menthol 4%. The panels include active ingredient, uses for minor aches and pains, warnings for external use only and flammability, stop use conditions, directions for adults and children, storage instructions, inactive ingredients, and a contact number for questions or comments.*

FDA Label Image

Full Carton Label (59316 209 Front Label)

Biofreeze Overnight Roll-on 40 mg/mL Menthol-Pain Relieving Gel packaging label showing two 2.5 fl oz (74 mL) bottles, totaling 5 fl oz (148 mL). The label highlights day & overnight relief with fast acting, long lasting menthol pain relief and lavender-scented overnight relief. Features include convenient roll-on, easy and mess-free application, and travel-friendly design. Manufactured by Reckitt Benckiser 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.