Hydrocortisone 0.5% / Hydroquinone 6% / Tretinoin 0.025%
Product Images NDC 72934-6104

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 0.025% (NDC 72934-6104). 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 (6104 2 End)

Close-up image of a white container label for a product from Sincerus Florida, LLC. The visible section includes directions for use stating it should be applied topically as directed by a physician, with instructions to wash hands after use and store at controlled room temperature (20-25°C). The label includes manufacturer contact information and a QR code. Product name and ingredient details are partially visible on the edge.*

FDA Label Image

V (6104 2 Front)

Packaging label of HYDROCORTISONE 0.5% / HYDROQUINONE 6% / TRETINOIN 0.025% emulsion, 30 gram tube by Sincerus Florida, LLC. The label includes the NDC number 72934-6104-2 and indicates this is a compounded drug made in the USA.*

FDA Label Image

Z (6104 2 Middle)

Label panel of HYDROCORTISONE 0.5% / HYDROQUINONE 6% / TRETINOIN 0.025% cream by Sincerus Florida, LLC showing the list of active ingredients with their strengths and inactive ingredients including Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning compounds, Edetate Disodium USP Dihydrate, Kojic Acid, 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.