Ciclopirox 3% / Itraconazole 5% / Urea 20%
Product Images NDC 72934-2044

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 Ciclopirox 3% / Itraconazole 5% / Urea 20% (NDC 72934-2044). 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.

Product Images & Figures Index

FDA Label Image

Ws (2 End)

Ws (2 End)
A product label panel showing directions for use of the medication labeled under Sincerus Florida, LLC. Instructions include to apply topically as directed by a physician, to wash hands after use, and to store at controlled room temperature (20-25°C). Contact information for reporting adverse reactions to Sincerus Florida, LLC and FDA is also provided, along with a QR code at the bottom.*
FDA Label Image

A (2044 2 Front)

A (2044 2 Front)
CICLOPIROX 3% / ITRACONAZOLE 5% / UREA 20% cream in a 30gm white container. The label shows the active ingredients with their strengths and the NDC number 72934-2044-2. It also displays the Sincerus Florida logo and text indicating it is a compounded drug made in the USA.*
FDA Label Image

Sd (2044 2 Middle)

Sd (2044 2 Middle)
The image shows a white cylindrical cream container label for CICLOPIROX 3% / ITRACONAZOLE 5% / UREA 20% cream by Sincerus Florida, LLC. The label includes a detailed list of active and inactive ingredients along with their USP percentages, and manufacturing details. The label states this is for Rx use only.*

* 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.