Salicylic Acid 2% /sodium Sulfacetamide Monohydrate 8%
Product Images NDC 72934-8170

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 2% /sodium Sulfacetamide Monohydrate 8% (NDC 72934-8170). 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

Wd (8170 7 End)

Wd (8170 7 End)
SALICYLIC ACID 2% / SODIUM SULFACETAMIDE MONOHYDRATE 8% in a white plastic bottle with a white screw cap. The visible label includes directions for use, contact information for Sincerus Florida, LLC in Pompano Beach, FL, and a QR code. The label instructs topical application and storage at controlled room temperature. No other branding or strength details are visible on the bottle.*
FDA Label Image

Cc (8170 7 Front)

Cc (8170 7 Front)
The image shows a white cylindrical bottle labeled as SALICYLIC ACID 2% and SODIUM SULFACETAMIDE MONOHYDRATE 8% suspension, 240 grams. The label includes the NDC number 72934-8170-7 and indicates the product is compounded by Sincerus Florida, LLC, made in the USA. The label also states it is for prescription use only.*
FDA Label Image

Sad (8170 7 Middle)

Sad (8170 7 Middle)
SALICYLIC ACID 2% / SODIUM SULFACETAMINE MONOHYDRATE 8% suspension bottle from Sincerus Florida, LLC. The white bottle displays a label listing the active ingredients salicylic acid USP 2% and sulfacetamide sodium monohydrate USP 8%, along with inactive ingredients. The lot number and manufacturing/BUD dates are also 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.