Hydrocortisone 2.5% / Hydroquinone 4% / Tretinoin 0.025%,
Product Images NDC 72934-6110

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 2.5% / Hydroquinone 4% / Tretinoin 0.025%, (NDC 72934-6110). 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

Efr (2 End)

Efr (2 End)
A white container side label showing directions for use of the topical medication. Instructions indicate to apply as directed by a physician, wash hands after use, and store at controlled room temperature (20-25°C). The label includes manufacturer contact information for Sincerus Florida, LLC in Pompano Beach, FL, with phone numbers and FDA reporting details.*
FDA Label Image

Dw (6110 2 Front)

Dw (6110 2 Front)
Packaging label of HYDROCORTISONE USP 2.5% / HYDROQUINONE USP 4% / TRETINOIN USP 0.025% emulsion in a 30gm container, labeled by Sincerus Florida, LLC. The label includes the NDC 72934-6110-2 and states it is a compounded drug made in the USA.*
FDA Label Image

Sfg (6110 2 Middle (inactives Only))

Sfg (6110 2 Middle (inactives Only))
Label panel of HYDROCORTISONE 2.5% / HYDROQUINONE 4% / TRETINOIN 0.025% product by Sincerus Florida, LLC showing inactive ingredients list. The label includes various inactive components with percentage amounts, including Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning 1501 and 9011, Edetate Disodium USP Dihydrate, Emulsifix, Krisgel 100, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF.*

* 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.