Benzoyl Peroxide 5% / Clindamycin1% / Niacinamide 2% / Tretinoin 0.025%
Product Images NDC 72934-1020

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Benzoyl Peroxide 5% / Clindamycin1% / Niacinamide 2% / Tretinoin 0.025% (NDC 72934-1020). 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

J (1020 2 End)

Back side label of a white cylindrical container showing directions for use and company contact information. The label advises to apply the product topically as directed by a physician, wash hands after use, and store at controlled room temperature (20-25°C). It also provides contact details for Sincerus Florida, LLC in Pompano Beach, FL, including phone numbers and a website for reporting adverse reactions.*

FDA Label Image

J (1020 2 Front)

Bottle label of BENZOYL PEROXIDE 5% / CLINDAMYCIN PHOSPHATE 1% / NIACINAMIDE 2% / TRETINOIN 0.025% gel, 30 grams, by Sincerus Florida, LLC. The label includes the NDC 72934-1020-2 and states it is a compounded drug made in the USA. A dual-colored logo with teal and orange sections and the words SINCERUS FLORIDA is visible.*

FDA Label Image

1020 2 Ingredients

Partial label of BENZOYL PEROXIDE 5% / CLINDAMYCIN 1% / NIACINAMIDE 2% / TRETINOIN 0.025% gel tube by Sincerus Florida, LLC. The label includes active ingredients imiquimod USP 5% and niacinamide USP 4%, and inactive ingredients such as glycerin USP, gel base, and tea tree oil. The label also shows a lot number, manufacturing date 06/01/2020, and BUD 01/27/2021.*

* 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.