Cooling Pain Relief Gel
Product Images NDC 72937-630

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cooling Pain Relief (NDC 72937-630). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunset Novelties, 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

Pr L4 (Fd 03678.1 Sunset Pain Relief Gel Whemp Oil 4 Floz 1000)

Pr L4 (Fd 03678.1  Sunset Pain Relief Gel Whemp Oil 4 Floz 1000)
Label for COOLING PAIN RELIEF Gel containing 3% camphor and 6% menthol, a topical analgesic by SUNSET NOVELTIES, INC. The front features an anatomical illustration highlighting pain relief areas with text noting hemp seed oil infusion and natural oils. The back includes Drug Facts detailing active ingredients, uses, warnings, directions, and inactive ingredients. The package size is 4 fl oz (118 mL).*
FDA Label Image

Cooling 8 Oz (Fd 03678.1 Sunset Pain Relief Gel Whemp Oil 8 Floz 2000)

Cooling 8 Oz (Fd 03678.1  Sunset Pain Relief Gel Whemp Oil 8 Floz 2000)
Label for COOLING PAIN RELIEF gel by SUNSET NOVELTIES, INC containing menthol 6% and camphor 3% as active ingredients. The front panel shows an anatomical illustration highlighting common pain sites and states 'Ultra Strength Pain Relief' and 'Temporary Cooling Relief of Sore Muscles'. The label indicates it contains 8 fl oz (236 mL) and is infused with rosemary, thyme, tea tree, and mint oil, plus 2000 hemp seed oil. The back panel includes Drug Facts, directions, warnings, inactive ingredients, and manufacturer contact information.*

* 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.