Verucide Wart Remover Kit
Product Images NDC 63347-720

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Verucide Wart Remover Kit (NDC 63347-720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blaine Labs 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.

FDA Label Image

Step1 Verucide (Step1 Verucide)

Step1 Verucide (Step1 Verucide)
Label for VeruCide Wart Remover Kit by Blaine Labs Inc., featuring the product name prominently with a physician formula indication. The label specifies Step 1 with a volume of 0.253 fl. oz. (7.5 ml) and includes directions to apply one or two drops, scrub with a brush, then rinse and dry thoroughly.*
FDA Label Image

Step2 Verucide (Step2 Verucide)

Step2 Verucide (Step2 Verucide)
The image shows a directional text panel for VeruCide Wart Remover Kit by Blaine Labs. It highlights Step 2 instructions, stating to dab the product directly onto the wart and allow it to dry. The volume indicated is 0.101 fl. oz. (3.0 ml), and the product is labeled as a physician formula.*
FDA Label Image

Verucide 750 Kit (Verucide 750 Kit)

Verucide 750 Kit (Verucide 750 Kit)
Box packaging label for VERUCIDE WART REMOVER Kit by Blaine Labs Inc. This two-step wart treatment kit contains salicylic acid in a solution with alcohol and papaya extract. The label includes Drug Facts, directions for use, inactive ingredients, manufacturer details, and product quantities (Step 1: 0.253 FL OZ, Step 2: 0.101 FL OZ). It is marked for exclusive physician dispensing and made in the USA.*

* 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.