Benzoyl Peroxide 2.5% / Clindamycin 1% / Niacinamide 2% / Tretinoin 0.025%
Product Images NDC 72934-1022

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 1% / Niacinamide 2% / Tretinoin 0.025% (NDC 72934-1022). 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)

Container for BENZOYL PEROXIDE 2.5% / CLINDAMYCIN 1% / NIACINAMIDE 2% / TRETINOIN 0.025% by Sincerus Florida, LLC. The label includes usage directions and contact information for reporting adverse reactions, specifying storage at controlled room temperature (20-25°C), external use only, and instructions to wash hands after use.*

FDA Label Image

Sf (1022 2 Front)

Packaging label of BENZOYL PEROXIDE 2.5% / CLINDAMYCIN 1% / NIACINAMIDE 2% / TRETINOIN 0.025% gel, 30 gm, from Sincerus Florida, LLC. The label displays the active ingredients with their USP concentrations, the product is identified as a compounded drug, and it is made in the USA.*

FDA Label Image

Ad (1022 2 Middle)

Drug label text panel listing active ingredients: Benzoyl Peroxide USP 2.5%, Clindamycin Phosphate USP 1%, Niacinamide USP 2%, and Tretinoin USP 0.025%. Inactive ingredients include Butylated Hydroxytoluene NF, Glycerin USP, Lavender Oil, Sodium Metabisulfite NF, and Suspensse Gel, with their respective concentrations. The label also notes RX only, BUD date, lot number, and manufacturer date details.*

* 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.