Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%
Product Images NDC 72934-6099

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 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025% (NDC 72934-6099). 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

C (6099 2 End)

C (6099 2 End)
Side view of a white cylindrical container label for HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% by Sincerus Florida, LLC. The label includes directions for use, contact information for reporting adverse reactions, and storage instructions to keep at controlled room temperature (20-25C).*
FDA Label Image

Z (6099 2 Front)

Z (6099 2 Front)
Label on a white cylindrical container for HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% emulsion, 30gm, with NDC 72934-6099-2. The label includes the text 'SINCERUS FLORIDA' flanking a stylized 'S' logo, and notes that this is a compounded drug made in the USA.*
FDA Label Image

X (6099 2 Middle)

X (6099 2 Middle)
Label of HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% showing the active and inactive ingredients with their concentrations. The label includes ingredients like Hydrocortisone USP, Hydroquinone USP, Tretinoin USP, and various inactive ingredients such as Citric Acid USP Anhydrous and Cyclomethicone. The label also displays the labeler as Sincerus Florida, LLC and contains NDC information.*

* 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.