Benzoyl Peroxide 5% / Clindamycin 1% / Niacinamide 4%
Product Images NDC 72934-1019

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 4% (NDC 72934-1019). 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

B (1013 2 End)

The image shows a white container with a label that includes directions for use and contact information for Sincerus Florida, LLC. The product is BENZOYL PEROXIDE 5% / CLINDAMYCIN 1% / NIACINAMIDE 4% by Sincerus Florida, LLC. The label instructs to use as directed by a physician, apply topically, and wash hands after use. It is for external use only and should be stored at controlled room temperature (20-25°C).*

FDA Label Image

V (1019 2 Front)

Label on a white container for BENZOYL PEROXIDE 5% / CLINDAMYCIN PHOSPHATE 1% / NIACINAMIDE 4% gel, 30gm. The label includes the product's NDC 72934-1019-2 and states it is a compounded drug made in the USA by Sincerus Florida, LLC, with their logo displayed in teal and orange colors.*

FDA Label Image

Hbnm (1019 2 Middle)

Label panel of BENZOYL PEROXIDE 5% / CLINDAMYCIN 1% / NIACINAMIDE 4% suspension gel showing active ingredients: Benzoyl Peroxide USP 5%, Clindamycin Phosphate USP 1%, Niacinamide USP 4%. Inactive ingredients include Butylated Hydroxytoluene NF, Glycerin USP, Krisgel 100, Lavender Oil, Sodium Metabisulfite NF. The label also lists lot number 011518ABCDEFGH and manufacture and expiration dates 01/01/1970.*

* 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.