Hydrocortisone 2.5% / Iodoquinol 1% / Ketoconazole 2%
Product Images NDC 72934-2111

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 Hydrocortisone 2.5% / Iodoquinol 1% / Ketoconazole 2% (NDC 72934-2111). 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

Ed (2 End)

Ed (2 End)
A white cylindrical container displaying a label with usage directions and contact information for Sincerus Florida, LLC. The label advises applying the product topically as directed by a physician, washing hands after use, and storing at controlled room temperature (20-25°C). It includes the manufacturer's address in Pompano Beach, FL and phone numbers for reporting adverse reactions and FDA contact.*
FDA Label Image

Z (2111 2 Front)

Z (2111 2 Front)
Packaging label of HYDROCORTISONE 2.5% / IODOQUINOL 1% / KETOCONAZOLE 2% cream, 30gm tube. The label displays the active ingredients with their concentrations and states it is a compounded drug. The labeler is Sincerus Florida, LLC, and the product is made in the USA.*
FDA Label Image

E (2111 2 Middle)

E (2111 2 Middle)
Close-up image of a white pharmaceutical container showing part of the product label for Hydrocortisone 2.5% / Iodoquinol 1% / Ketoconazole 2% cream. Label details visible include active ingredient concentrations and inactive ingredient Lipobase Heavy at 94.5%. Additional label text references Rx only status, BUD and MFG dates, lot number, and partial manufacturer information for Sincerus Florida, LLC.*

* 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.