Benzoyl Peroxide 8% / Niacinamide 4%
Product Images NDC 72934-8022

3 FDA label images from Sincerus Florida · 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 8% / Niacinamide 4% (NDC 72934-8022). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, 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

D (8022 6 End)

D (8022 6 End)
Bottle label of BENZOYL PEROXIDE 8% / NIACINAMIDE 4% by Sincerus Florida. The label includes directions for use advising application as directed by a physician, topical use only, and instructions to wash hands after use. Storage instructions specify controlled room temperature (20-25°C). Manufacturer contact information is provided.*
FDA Label Image

S (8022 6 Front)

S (8022 6 Front)
White plastic bottle with a flip-top cap containing BENZOYL PEROXIDE 8% / NIACINAMIDE 4% suspension, 120 gm. The label shows the product's NDC 72934-8022-6 and includes the Sincerus Florida logo in teal and orange. The label indicates that this is a compounded drug made in the USA.*
FDA Label Image

D (8022 6 Middle)

D (8022 6 Middle)
The image shows a white cylindrical bottle with a flip-top cap containing BENZOYL PEROXIDE 8% / NIACINAMIDE 4% suspension by Sincerus Florida. The label lists active ingredients benzoyl peroxide USP 8% and niacinamide USP 4%, as well as inactive ingredients including cocamide DEA, diethylene glycol monoethyl ether NF, and suspensse shampoo. The label also includes manufacturing and lot 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.