Hydrocortisone 0.5% / Hydroquinone 6%
Product Images NDC 72934-6103

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% (NDC 72934-6103). 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

Asd (2 End)

Asd (2 End)
Side view of a white cylindrical bottle label for HYDROCORTISONE 0.5% / HYDROQUINONE 6% by Sincerus Florida, LLC. The label includes directions for use, storage instructions at controlled room temperature (20-25°C), and contact information for reporting adverse reactions to Sincerus Florida, LLC, including a phone number and FDA MedWatch website. The label indicates the product is for external use only and office use only.*
FDA Label Image

Dg (6103 2 Front)

Dg (6103 2 Front)
HYDROCORTISONE 0.5% / HYDROQUINONE 6% emulsion in a 30 gm container from Sincerus Florida, LLC. The white cylindrical bottle label includes product strengths and notes it is a compounded drug made in the USA.*
FDA Label Image

Df (6103 2 Middle)

Df (6103 2 Middle)
Side panel text listing active and inactive ingredients of HYDROCORTISONE 0.5% / HYDROQUINONE 6%. Active ingredients include hydrocortisone USP 0.5% and hydroquinone USP 6%. Inactive ingredients include ascorbyl palmitate FCC, citric acid USP anhydrous, cyclomethicone, Dow Corning 1501 and 9011, edetate disodium USP dihydrate, green tea extract, kojic acid, purified water USP, sodium chloride USP, sodium metabisulfite NF, and vitamin E acetate USP liquid.*

* 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.