Dapsone 8.5% / Niacinamide 2% / Spironolactone 5%
Product Images NDC 72934-1064

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 8.5% / Niacinamide 2% / Spironolactone 5% (NDC 72934-1064). 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

De (2 End)

De (2 End)
Side view of a white cylindrical container housing DAPSONE 8.5%, NIACINAMIDE 2%, SPIRONOLACTONE 5% topical product by Sincerus Florida, LLC. The label includes directions for use and contact information for reporting adverse reactions, along with a QR code near the bottom.*
FDA Label Image

A (1064 2 Front)

A (1064 2 Front)
The image shows a white cylindrical container labeled DAPSONE USP 8.5%, NIACINAMIDE USP 2%, SPIRONOLACTONE USP 5% gel in a 30gm size. The label includes the NDC number 72934-1064-2 and the name of the labeler, Sincerus Florida, LLC. It states the product is a compounded drug made in the USA.*
FDA Label Image

Dw (1064 2 Middle)

Dw (1064 2 Middle)
Partial label on a white cylindrical container showing active and inactive ingredient details. Active ingredients listed include Dapsone USP 8.5%, Niacinamide USP 2%, and Spironolactone USP 5%. Inactive ingredients visible include Lavender Oil 0.25%, Propylene Glycol USP 5%, and Suspendsse Gel 79.25%. The label also indicates this is Rx only and provides BUD, lot number, and manufacturing 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.