Medicated Anti-itch
Product Images NDC 0363-3231

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Medicated Anti-itch (NDC 0363-3231). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreens, 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 Description (Back)

Drug Facts panel for MEDICATED ANTI-ITCH Well at Walgreens lists active ingredients Menthol 1% as pain reliever and Pramoxine Hydrochloride 1% as external analgesic. It details uses for relief of pain and itching from minor burns, sunburn, scrapes, skin irritations, minor cuts, and rashes. Warnings emphasize external use only, avoiding contact with eyes, and consulting a doctor if condition worsens. Directions specify application limits for adults and children 2 years and older; consult a doctor for younger children. Inactive ingredients and storage instructions are also provided.*

FDA Label Image

Image Description (Front)

Packaging label for MEDICATED ANTI-ITCH Well at Walgreens maximum strength cream enriched with aloe and vitamin E. The label highlights fast-acting, cooling relief and mentions it relieves pain and itch. The net weight is 2 oz (56 g). The label includes Walgreens branding and a barcode, along with distributor information from Walgreen Co., Deerfield, IL.*

* 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.