Pain Relief Gel
Product Images NDC 73672-989

2 FDA label images from Hempfusion, Inc. · 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 Pain Relief Gel (NDC 73672-989). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hempfusion, 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 (Hf Painrelief Gel Label V1.3 Pantone Outlined Page 001)

Bottle (Hf  Painrelief  Gel Label  V1.3  Pantone  Outlined Page 001)
Label for Pain Relief Gel by HempFusion, Inc. The gel contains menthol 1.5% as the active ingredient. The label includes drug facts such as uses for temporary relief of minor aches and pains of muscles and joints, warnings about external use only, and directions for use by adults and children 12 years or older. It also lists inactive ingredients including water, glycerin, peppermint oil, hemp extracts, aloe leaf juice, arnica flower extract, and others. The product is non-GMO, suitable for all skin types, and comes in a 50 mL (1.69 fl oz) container.*
FDA Label Image

Carton (Otc Pain Relief Gel Carton Flat V1.7 00816179029847 Page 001)

Carton (Otc Pain Relief Gel Carton Flat  V1.7 00816179029847 Page 001)
Packaging label for Pain Relief Gel Menthol 1.5% by HempFusion, Inc. The label highlights the active ingredient menthol, mentions the inclusion of moisturizing Arnica, hemp extract, naturally occurring CBD, and terpenes, and states it is non-GMO and suitable for all skin types. The label features usage directions, warnings, a list of ingredients, the company's contact information, and a barcode. The product size is 50 mL (1.69 fl oz).*

* 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.