Ketoconazole 2% / Niacinamide 4%
Product Images NDC 72934-2132

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ketoconazole 2% / Niacinamide 4% (NDC 72934-2132). 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

K (2 End)

Packaging label of KETOCONAZOLE 2% / NIACINAMIDE 4% by Sincerus Florida LLC showing part of the container with usage directions. The label instructs to apply topically as directed by a physician, wash hands after use, and store at controlled room temperature. It also includes contact information for Sincerus Florida LLC and FDA reporting details.*

FDA Label Image

S (2132 2 Front)

KETOCONAZOLE 2% / NIACINAMIDE 4% cream in a 30gm white cylindrical container. The label shows the product NDC 72934-2132-2 and features the Sincerus Florida LLC logo. The product is identified as a compounded drug made in the USA.*

FDA Label Image

F (2132 2 Middle)

KETOCONAZOLE 2% / NIACINAMIDE 4% cream bottle label from Sincerus Florida LLC. The label lists active ingredients as Ketoconazole USP 2% and Niacinamide USP 4%, with inactive ingredients comprising 94%. Manufacturing and expiration details are partially visible, including a lot number and dates.*

* 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.