Salonpas Arthritis Pain Patch
Product Images NDC 46581-680

2 FDA label images from Hisamitsu Pharmaceutical Co., 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 Salonpas Arthritis Pain (NDC 46581-680). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hisamitsu Pharmaceutical Co., 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

Image Of 20-patch Box Label (4658168020 1)

Image Of 20-patch Box Label (4658168020 1)
Salonpas Arthritis Pain Patch packaging showing the product name, active ingredients Menthol 3% and Methyl Salicylate 10%, and its use as a topical analgesic for arthritis, joint pain, sprains, and strains. It indicates application for 8-12 hours, contains 20 patches sized 7 cm by 10 cm, and is labeled by Hisamitsu Pharmaceutical Co., Inc. The label includes a caution about not using more than one patch at a time and keeping out of reach of children.*
FDA Label Image

Image Of 1-patch Sample Pouch Label (4658168099 3)

Image Of 1-patch Sample Pouch Label (4658168099 3)
The Salonpas Arthritis Pain Patch packaging label shows a 1-patch package with a patch size of about 7cm x 10cm. The topical analgesic patch contains 3% Menthol and 10% Methyl Salicylate for temporary relief of mild to moderate pain, including arthritis, joint pain, sprains, and strains. Instructions include peeling the center film and placing the patch on the affected area. It is FDA-approved as a non-prescription pain-relieving patch, manufactured by Hisamitsu Pharmaceutical Co., Inc. in Japan and distributed by Hisamitsu America, Inc.*

* 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.