Itch Relief Gel
Product Images NDC 13709-351

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Itch Relief (NDC 13709-351). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Neilmed Pharmaceuticals 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.

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FDA Label Image

Itch Relief (Itchrelief)

Itch Relief (Itchrelief)
This text contains information about a topical analgesic product with 2% diphenhydramine hydrochloride as the active ingredient. It is indicated for temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, skin irritations, and rashes from poison ivy, oak, and sumac. The product is for external use only and should not be used on large areas of the body or in combination with other diphenhydramine-containing products taken orally. Directions for use are provided for adults and children. The formulation includes inactive ingredients such as camphor, urea, hydroxyethyl cellulose, and various parabens. It also lists contact information for inquiries or questions. The text also includes a comparison to another product called Benadryl Extra Strength Topical Analgesic Itch Stopping Gel. The manufacturer's details are provided along with temperature storage instructions.*

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