Hydrocortisone 2.5% / Ketoconazole 2%
Product Images NDC 72934-2112

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydrocortisone 2.5% / Ketoconazole 2% (NDC 72934-2112). 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

S (2 End)

Side view of a white cylindrical container for HYDROCORTISONE 2.5% / KETOCONAZOLE 2% topical product by Sincerus Florida, LLC. The label includes directions for use, storage instructions, and contact information for adverse reaction reporting, along with a QR code.*

FDA Label Image

C (2112 2 Front)

Packaging label of HYDROCORTISONE 2.5% / KETOCONAZOLE 2% cream in a 30 gm container. The label displays the NDC 72934-2112-2 and states the product is a compounded drug. The label includes the Sincerus Florida logo and indicates the product is made in the USA.*

FDA Label Image

Ss (2112 2 Middle)

Side view of a white tube labeled with the active ingredients and their concentrations for a medicinal cream. The label shows Hydrocortisone USP at 2.5% and Ketoconazole USP at 2% as active ingredients, and Lipobase Heavy as an inactive ingredient at 95.5%. It includes manufacturing and lot information, indicating a prescription-only product from 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.