Salicylic Acid 5% / Sodium Sulfacetamide Monohydrate 10%
Product Images NDC 72934-8172

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 Salicylic Acid 5% / Sodium Sulfacetamide Monohydrate 10% (NDC 72934-8172). 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

S (8172 6 End)

S (8172 6 End)
Back label of SALICYLIC ACID 5% / SODIUM SULFACETAMIDE MONOHYDRATE 10% bottle by Sincerus Florida, LLC. The white cylindrical bottle shows directions for use, including physician guidance, topical application, and storage at controlled room temperature. Manufacturer contact information and a QR code are also visible on the label.*
FDA Label Image

Z (8172 6 Front)

Z (8172 6 Front)
White plastic bottle label for SALICYLIC ACID USP 5% and SULFACETAMIDE SODIUM MONOHYDRATE USP 10% suspension, 120gm, from Sincerus Florida, LLC. The label includes NDC 72934-8172-6, states it is a compounded drug, and indicates it is made in the USA. The label also shows the manufacture and expiration date and the lot number.*
FDA Label Image

D (8172 6 Middle)

D (8172 6 Middle)
Bottle label of SALICYLIC ACID 5% / SODIUM SULFACETAMIDE MONOHYDRATE 10% suspension shampoo by Sincerus Florida, LLC. The label lists active ingredients Salicylic Acid USP 5% and Sulfacetamide Sodium Monohydrate USP 10%, along with inactive ingredients Cocamide DEA 2%, Propylene Glycol USP 8%, Sulfur Precipitated USP 2.75%, and Suspension Shampoo 72.25%. The label also includes lot number, manufacturing, and expiration 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.