Benzoyl Peroxide 2.5% / Clindamycin 1% / Niacinamide 4%
Product Images NDC 72934-1013

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 1% / Niacinamide 4% (NDC 72934-1013). 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

G (1013 2 End)

G (1013 2 End)
Side label of a white cylindrical container for BENZOYL PEROXIDE 2.5% / CLINDAMYCIN 1% / NIACINAMIDE 4% by Sincerus Florida, LLC. Label includes directions for use and contact information for reporting adverse reactions, with a small QR code at the bottom left.*
FDA Label Image

S (1013 2 Front)

S (1013 2 Front)
Packaging label of Benzoyl Peroxide USP 2.5%, Clindamycin Phosphate USP 1%, Niacinamide USP 4% gel in a 30 gm white container. The label displays the NDC 72934-1013-2 and the manufacturer's logo for Sincerus Florida, LLC. It states the product is a compounded drug made in the USA.*
FDA Label Image

D (1013 2 Middle)

D (1013 2 Middle)
Side view of a white cylindrical container label showing the active ingredients of BENZOYL PEROXIDE 2.5% / CLINDAMYCIN 1% / NIACINAMIDE 4% gel, including Benzoyl Peroxide USP 2.5%, Clindamycin Phosphate USP 1%, and Niacinamide USP 4%. The label also lists inactive ingredients such as Butylated Hydroxytoluene NF, Glycerin USP, Lavender Oil, and Suspensisse Gel, along with batch and manufacture information.*

* 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.