Anti Itch Cream
Product Images NDC 41250-622

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Anti Itch (NDC 41250-622). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meijer Distribution 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

622 6e Anti Itch Cream Image

622 6e Anti Itch Cream Image
This is a description of an Extra Strength anti-itch cream that provides fast relief for most outdoor itches including insect bites and skin irritations from poison ivy, oak, and sumac. The cream contains Diphenhydramine Hydrochloride 2% and Zinc Acetate 0.1 which temporarily relieve pain and itching due to minor skin irritations. It is for external use only and should not be used on larger parts of the body nor with another product containing diphenhydramine, even one taken by mouth. The cream should be used no more than 3 to 4 times daily for adults and children over 2 years, while children under 2 years should consult a physician. It is not manufactured or distributed by Johnson & Johnson, owner of the registered trademark Benadryl. The inactive ingredients include cetyl alcohol, Dazolidinyl Urea, methylparaben, PEG-2 stearate, PEG 20 stearate, Propylene Glycol, propylparaben, and purified water.*

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