Benzoyl Peroxide 5% / Clindamycin 1% / Niacinamide 2% / Spironolactone 2%
Product Images NDC 72934-1014

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Benzoyl Peroxide 5% / Clindamycin 1% / Niacinamide 2% / Spironolactone 2% (NDC 72934-1014). 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)

The image shows a white cylindrical container with a label that includes directions for use and contact information for Sincerus Florida, LLC, located in Pompano Beach, FL. The label instructs to apply the product topically, for external use only, and to wash hands after use. It also includes storage instructions and a QR code. The product corresponds to BENZOYL PEROXIDE 5% / CLINDAMYCIN 1% / NIACINAMIDE 2% / SPIRONOLACTONE 2% by Sincerus Florida, LLC.*

FDA Label Image

Ad (1014 2 Front)

Packaging label of BENZOYL PEROXIDE 5% / CLINDAMYCIN PHOSPHATE 1% / NIACINAMIDE 2% / SPIRONOLACTONE 2% gel, 30 gm, by Sincerus Florida, LLC. The label includes the NDC number 72934-1014-2 and states it is a compounded drug made in the USA. The label features the Sincerus Florida logo in teal and orange colors.*

FDA Label Image

R (1014 2 Middle)

Partial label on a white cylindrical container displaying active ingredients Benzoyl Peroxide USP 5%, Clindamycin Phosphate USP 1%, Niacinamide USP 2%, and Spironolactone USP 2%, along with inactive ingredients including Glycerin USP, Lavender Oil, and other components. Also visible are Rx only designation, BUD and manufacturing dates, and a lot number.*

* 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.