Cantharidin 1% / Podophyllum Resin 5% / Salicylic Acid 30%
Product Images NDC 72934-9036

3 FDA label images from Sincerus Florida, Llc · 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 Cantharidin 1% / Podophyllum Resin 5% / Salicylic Acid 30% (NDC 72934-9036). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, Llc, 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

Ds (9036 9 Adverse)

Ds (9036 9 Adverse)
Brown plastic bottle with a black ribbed cap displaying a product label for CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30% by Sincerus Florida, LLC. The label shows partial text including manufacturer information, contact details, and a QR code. A document with a table of inactive ingredients is partially visible in the background.*
FDA Label Image

Sdf (9036 9 Front)

Sdf (9036 9 Front)
Packaging label on an amber plastic bottle with a black ribbed cap for CANTHARIDIN 1% / PODOPHYLLUM RESIN USP 5% / SALICYLIC ACID USP 30% liquid 15gm. The label includes the product NDC 72934-9036-9, the labeler Sincerus Florida, LLC, and states the product is a compounded drug made in the USA.*
FDA Label Image

Sd (9036 9 Middle And Instructions For Use)

Sd (9036 9 Middle And Instructions For Use)
Brown glass bottle with black ribbed cap showing a white label that lists active and inactive ingredients including Cantharidin 1%, Podophyllum Resin 5%, and Salicylic Acid 30%. The label also includes directions for use, manufacturer information for Sincerus Florida, LLC, and a QR code. The bottle is upright against a plain white background.*

* 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.