Pain Relief Gel-roll On
Product Images NDC 83016-331

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pain Relief Gel-roll On (NDC 83016-331). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by R & Y Group, 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

Bottle Label (83016 331 01)

PAIN RELIEF Gel-Roll On by R & Y Group, LLC is a 2.5 fl oz (74 mL) roll-on topical analgesic containing Menthol 4%. The blue label highlights fast-acting, easy application, and no-mess roll-on features for temporary pain relief. The label includes drug facts, warnings, directions, inactive ingredients, and manufacturer information. It states the product is made in China and supports Susan G. Komen.*

FDA Label Image

Bag Label (83016 331 11)

Packaging label for PAIN RELIEF Gel-Roll On by R & Y Group, LLC. The label highlights the product as a topical analgesic with 4% menthol for cold therapy pain relief targeting sore muscles, backaches, joints, bruises, and arthritis. It provides usage directions, warnings, inactive ingredients, and manufacturer information, including social media handles and a Susan G. Komen partnership statement.*

FDA Label Image

21 (83016 331 21)

Packaging label for PAIN RELIEF Gel-Roll On by R & Y Group LLC, featuring TherICE branding. The label highlights topical analgesic gel with 4% menthol active ingredient, designed for temporary relief of minor aches and pains of muscles and joints. The label includes warnings, directions, inactive ingredients, manufacturer details, social media handles, and a barcode.*

* 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.