011503 Dapsone 6% / Niacinamide 2% / Spironolactone 5%
Product Images NDC 72934-1211

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 011503 Dapsone 6% / Niacinamide 2% / Spironolactone 5% (NDC 72934-1211). 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

W (2 End)

W (2 End)
A label panel showing directions for use of 011503 DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5% topical product by Sincerus Florida, LLC. It advises use as directed by a physician, with instructions to apply topically and wash hands after use. The product is for external use only and should be stored at controlled room temperature (20-25°C). Contact information for reporting adverse reactions is also provided.*
FDA Label Image

D (1211 2 Front)

D (1211 2 Front)
Close-up of a white cylindrical container label for 011503 DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5% gel 30gm by Sincerus Florida, LLC. The label shows the NDC 72934-1211-2, and a logo with 'SINCERUS' and 'FLORIDA' in blue and orange colors respectively. Text indicates it is a compounded drug made in the USA.*
FDA Label Image

S (1211 2 Middle)

S (1211 2 Middle)
Packaging label of 011503 DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5% gel by Sincerus Florida, LLC. The visible portion shows active and inactive ingredient percentages, listing Dapsone USP 6%, Niacinamide USP 2%, and Spironolactone USP 5%, along with inactive ingredients such as Butylated Hydroxytoluene NF, Lavender Oil, and Propylene Glycol USP.*

* 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.