Benzoyl Peroxide 5% / Niacinamide 2% / Tretinoin 0.025%
Product Images NDC 72934-1021

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 5% / Niacinamide 2% / Tretinoin 0.025% (NDC 72934-1021). 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

C (2 End)

C (2 End)
A white cylindrical container with a label showing directions for use and contact information for Sincerus Florida, LLC, located in Pompano Beach, FL. The label includes instructions to use as directed by a physician, to apply topically, and to wash hands after use. It specifies storage at controlled room temperature (20-25°C) and provides FDA contact details for reporting adverse reactions.*
FDA Label Image

1021 2 Ingredients

1021 2 Ingredients
Close-up of a white cylindrical container label showing active and inactive ingredient information for BENZOYL PEROXIDE 5% / NIACINAMIDE 2% / TRETINOIN 0.025%. The label lists Benzoyl Peroxide USP 7.14%, Niacinamide USP 2%, and Tretinoin USP 0.025% as active ingredients. Inactive ingredients include Butylated Hydroxytoluene NF, Glycerin USP, Krisgel 100, Lavender Oil, and Sodium Metabisulfite NF.*
FDA Label Image

G (1021 2 Front)

G (1021 2 Front)
Label of BENZOYL PEROXIDE 5% / NIACINAMIDE 2% / TRETINOIN 0.025% gel in a 30gm container. The label shows the active ingredient strengths and indicates the product is a compounded drug made in the USA by Sincerus, Florida, LLC. The NDC number 72934-1021-2 is also visible.*

* 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.