Hydrocortisone 0.5% / Hydroquinone 8% / Tretinoin 0.025%
Product Images NDC 72934-6106

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 8% / Tretinoin 0.025% (NDC 72934-6106). 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

X (6106 2 End)

X (6106 2 End)
Side label of HYDROCORTISONE 0.5% / HYDROQUINONE 8% / TRETINOIN 0.025% cream or ointment container from Sincerus Florida, LLC. The label includes directions for use advising to apply topically as directed by a physician and lists the product as for external use only. Contact information for Sincerus Florida, LLC and FDA adverse reaction reporting details are included.*
FDA Label Image

C (6106 2 Front)

C (6106 2 Front)
Packaging label of HYDROCORTISONE 0.5% / HYDROQUINONE 8% / TRETINOIN 0.025% emulsion, 30gm, by Sincerus Florida, LLC. The label shows active ingredients with their USP concentrations and notes that this is a compounded drug made in the USA. The NDC number 72934-6106-2 is also displayed.*
FDA Label Image

X (6106 2 Middle)

X (6106 2 Middle)
Active and inactive ingredients panel for HYDROCORTISONE 0.5% / HYDROQUINONE 8% / TRETINOIN 0.025% topical drug by Sincerus Florida, LLC. Lists active ingredients hydrocortisone USP 0.5%, hydroquinone USP 8%, tretinoin USP 0.025%, plus various inactive ingredients including citric acid, cyclomethicone, and purified water.*

* 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.