Topical Analgesic
Product Images NDC 82165-104

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Topical Analgesic (NDC 82165-104). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dermaline Usa Corp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Label (Arnica Gel Expand New Out)

Label (Arnica Gel Expand New Out)
Wenthol 1% Topical Analgesic is a fast-acting formula that is helpful in temporarily relieving pain and discomfort related to sunburn, minor cuts, scrapes, insect bites, and minor skin irritation. This topical analgesic is for external use only, and it should be kept away from flames. Avoid contact with eyes and do not use on children under 16 years of age without the advice of a physician. If the condition worsens or symptoms persist for more than seven days or clear up and occur again within a few days, stop using Wenthol and consult a doctor. Always keep it out of reach of children, and if accidentally ingested, seek medical help or contact Poison Control Center immediately. The product is distributed by Dermaline USA, and additional product details can be found on dermalineuss.com. The formula contains Amica Exiact Camphor, Carbome, Deonized water, Do Hycatoin, Etyt Acohol, Eucalyptus O, Isopropyl Acohol, Nonaignok, Polysorate 20, Propylenegiyco, Tea Tree Oil as inactive ingredients. Store Wenthol at room temperature between 15 - 30 degrees Celsius (55:66 degrees Fahrenheit). If you have any questions, contact Dermaline USA at 1(800) 710-171.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.