Arex Sinsin Pas Patch
Product Images NDC 55264-021

2 FDA label images from Sinsin Pharmaceutical Co., Ltd. · 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 Arex Sinsin Pas (NDC 55264-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sinsin Pharmaceutical Co., Ltd., 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

9650380e 2c06 140a E053 2a95a90aaba5

9650380e 2c06 140a E053 2a95a90aaba5
Packaging label for Arex Sinsin Pas patch, a topical pain relieving patch with a cooling and heating effect. The front of the label shows the product name Arex with indication for joint pain, muscle pain, sprains, and backache. It includes details of cooling and heating effects, adherence, and flexibility. The label states the package contains 6 large patches. The back side features a Drug Facts box listing active ingredients including DL-Camphor, L-Menthol, Mentha Oil, Methyl Salicylate, and Zinc Oxide, purpose as topical analgesic, warnings, directions, and other information. The labeler is Sinsin Pharmaceutical Co., Ltd., and it is made in Korea.*
FDA Label Image

Arex Large

Arex Large
Packaging label for Arex Sinsin Pas patch, a topical analgesic patch with active ingredients including DL-Camphor 34.1 mg, L-Menthol 90.9 mg, Mentha Oil 45.46 mg, Methyl Salicylate 90.9 mg, and Zinc Oxide 431.82 mg. The label features the brand name AREX with Cool Hot branding, highlights pain relief for joint pain, muscle pain, sprains, and backache, and includes usage instructions and drug facts. The manufacturer is Sinsin Pharmaceutical Co., Ltd. and the NDC is 55264-021.*

* 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.