Verrustat Wart Remover Liquid
Product Images NDC 44577-020

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Verrustat Wart Remover (NDC 44577-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinical Therapeutic Solutions, 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

Verrustatliquidbottle (Verrustatliquidbottle)

FDA Label Image

Verrustatliquidbox (Verrustatliquidbox)

Verrustatliquidbox (Verrustatliquidbox)
VerruStat Liquid Wart Remover is a drug that contains Salicylic Acid 17%, which is used to remove common and plantar warts. The product is intended for external use only and should not be used on irritated or infected skin, moles, birthmarks, genital warts, or warts on the face or mucous membranes. The product is flammable, so it should be kept away from fire or flame. The directions for use involve washing or soaking the affected area and applying the wart remover liquid with an enclosed applicator. The procedure can be repeated once or twice a day until the wart is completely removed for up to 12 weeks. The product is stored at room temperature and contains other ingredients such as Butyl Acetate, Ethyl Acetate, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Nitrocellulose, Retinyl Palmitate, and SD-Alcohol 408. It comes in a 15 ml bottle with an applicator brush and is dispensed only by physicians.*

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