Benzoyl Peroxide 2.5%, Clindamycin Phosphate 1%, Niacinamide 2% / Tretinoin 0.05%
Product Images NDC 72934-1012

3 FDA label images from Sincerus Florida, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Benzoyl Peroxide 2.5%, Clindamycin Phosphate 1%, Niacinamide 2% / Tretinoin 0.05% (NDC 72934-1012). 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.

Product Images & Figures Index

FDA Label Image

Ed (2 End)

Ed (2 End)
Directions for use and labeler contact information on a white cylindrical container for BENZOYL PEROXIDE 2.5%, CLINDAMYCIN PHOSPHATE 1%, NIACINAMIDE 2% / TRETINOIN 0.05%. Instructions include application guidelines and storage conditions. The labeler is Sincerus Florida, LLC, with phone numbers and website information for adverse reaction reporting.*
FDA Label Image

Sf (1012 2 Front)

Sf (1012 2 Front)
Bottle label of BENZOYL PEROXIDE 2.5%, CLINDAMYCIN PHOSPHATE 1%, NIACINAMIDE 2%, and TRETINOIN 0.05% gel. The label indicates a 30gm compound drug supplied by Sincerus Florida, LLC, made in the USA, with NDC 72934-1012-2.*
FDA Label Image

Ds (1012 2 Middle)

Ds (1012 2 Middle)
Label on a white pharmaceutical container listing the active ingredients of benzoyl peroxide 2.5%, clindamycin phosphate 1%, niacinamide 2%, and tretinoin 0.05%, along with inactive ingredients including butylated hydroxytoluene, glycerin USP, lavender oil, sodium metabisulfite NF, and a gel base. The label includes manufacturing and lot information, associated with 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.