Desoximetasone 0.05% / Hydroquinone 6% / Tretinoin 0.05%
Product Images NDC 72934-6067

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Desoximetasone 0.05% / Hydroquinone 6% / Tretinoin 0.05% (NDC 72934-6067). 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

As (2 End)

Side view of a white cylindrical container with a label showing directions for use and company contact information. The label includes instructions for topical application, storage conditions (20-25°C), and advises washing hands after use. The label lists Sincerus Florida, LLC in Pompano Beach, FL, along with a phone number and FDA contacts for reporting adverse reactions. A small QR code is also visible.*

FDA Label Image

Qq (6067 2 Front)

DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05% emulsion in a 30gm white plastic container. The label includes NDC 72934-6067-2 and the logo of Sincerus Florida, LLC. The product is identified as a compounded drug made in the USA.*

FDA Label Image

Sdf (6067 2 Middle)

Label on a white cylindrical container listing active and inactive ingredients for DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05%. The active ingredients include Desoximetasone USP 0.05%, Hydroquinone USP 6%, and Tretinoin USP 0.05%. Inactive ingredients listed include Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning 1501, Dow Corning 9011, Edetate Disodium USP Dihydrate, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF, with their respective percentages.*

* 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.