Hydrocortisone 0.5% / Hydroquinone 6% / Tretinoin 0.05%
Product Images NDC 72934-6177

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 6% / Tretinoin 0.05% (NDC 72934-6177). 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

Ds (2 End)

Ds (2 End)
Side view of a white cylindrical container with a label showing directions for use and contact information for Sincerus Florida, LLC, the labeler of HYDROCORTISONE 0.5% / HYDROQUINONE 6% / TRETINOIN 0.05%. The label includes instructions for external topical application and a storage temperature range of 20-25°C.*
FDA Label Image

Fs (6177 2 Front)

Fs (6177 2 Front)
Packaging label of HYDROCORTISONE 0.5% / HYDROQUINONE 6% / TRETINOIN 0.05% emulsion 30gm by Sincerus Florida, LLC. The label displays the NDC 72934-6177-2 and states the product is a compounded drug made in the USA. The label includes the Sincerus Florida logo in blue and orange colors.*
FDA Label Image

Zx (6177 2 Middle)

Zx (6177 2 Middle)
A white container label for HYDROCORTISONE 0.5% / HYDROQUINONE 6% / TRETINOIN 0.05% by Sincerus Florida, LLC. The label details active ingredients including Hydrocortisone USP 0.5%, Hydroquinone USP 6%, and Tretinoin USP 0.05%, as well as inactive ingredients such as Citric Acid USP Anhydrous, Cyclomethicone, and others. It includes manufacturing and lot information towards the top right.*

* 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.