Dapsone 6% / Niacinamide 2% / Spironolactone 5%
Product Images NDC 72934-1061

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 Dapsone 6% / Niacinamide 2% / Spironolactone 5% (NDC 72934-1061). 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

D (2 End)

D (2 End)
Side view of a white container for DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5% topical product by Sincerus Florida, LLC. The label displays directions for use, including washing hands after application, storage at controlled room temperature (20-25°C), and contact information for reporting adverse reactions to Sincerus Florida, LLC.*
FDA Label Image

Sf (1061 2 Front)

Sf (1061 2 Front)
The image shows a white cylindrical container labeled with DAPSONE USP 6%, NIACINAMIDE USP 2%, and SPIRONOLACTONE USP 5% gel, 30 grams. The label includes the NDC number 72934-1061-2 and features the Sincerus Florida logo. It states that this is a compounded drug made in the USA.*
FDA Label Image

S (1061 2 Middle)

S (1061 2 Middle)
Label of DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5% gel by Sincerus Florida, LLC showing detailed active and inactive ingredient percentages. Active ingredients include Dapsone USP (6%), Niacinamide USP (2%), Spironolactone USP (5%). Inactive ingredients listed include Lavender Oil, Butylated Hydroxytoluene NF (BHT), Propylene Glycol USP, and Suspensisse Gel with their respective percentages. Manufacturing and expiration dates are also partially 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.