Stopain Extra Strength Gel
Product Images NDC 63936-8800

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Stopain Extra Strength Gel (NDC 63936-8800). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Troy Manufacturing, Inc., 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 (Bottle)

Bottle (Bottle)
Stopain Extra Strength Pain Relieving Gel 80 mg/mL (Menthol) topical analgesic gel in a 16 fl oz (473 mL) container. The label highlights fast-acting, long-lasting pain relief for arthritis, muscle aches, joint and back pain, with MSM and glucosamine. Manufactured by Troy Healthcare, LLC in the USA.*
FDA Label Image

Bottle2 (Bottle2)

Bottle2 (Bottle2)
Label of Stopain Extra Strength Pain Relieving Gel, topical gel containing menthol 80 mg/mL. The label highlights relief for arthritis, muscle aches, and joint & back pain, with MSM & glucosamine. The package size is 32 FL OZ (946 mL) and is manufactured by Troy Healthcare, LLC. The label includes a Drug Facts panel and contact information.*
FDA Label Image

Bottle3 (Bottle3)

Bottle3 (Bottle3)
Stopain Extra Strength Pain Relieving Gel packaging label, featuring the brand name prominently. The label highlights the product as a topical gel with MSM and glucosamine, intended for arthritis, muscle aches, joint, and back pain relief. The Drug Facts panel lists menthol 8.0% as the active ingredient. It is manufactured by Troy Healthcare, LLC, with an embossed logo and a barcode present. The label also notes key features such as long-lasting application, non-greasy, non-staining, and fast absorption.*

* 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.