Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%
Product Images NDC 72934-6102

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 4% / Tretinoin 0.025% (NDC 72934-6102). 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.

Product Images & Figures Index

FDA Label Image

Zdb (2 End)

Zdb (2 End)
Side view of a white cylindrical container labeled with directions for use and company contact information. The text instructs to apply topically as directed by a physician and to wash hands after use, specifying storage at controlled room temperature (20-25°C). The label lists Sincerus Florida, LLC as the labeler based in Pompano Beach, FL, and includes contact phone numbers and FDA reporting information with a QR code at the bottom.*
FDA Label Image

Fsh (6102 2 Front)

Fsh (6102 2 Front)
Label on a white container for HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% emulsion, 30 gm, from Sincerus Florida, LLC. The label shows the NDC number 72934-6102-2 and states it is a compounded drug made in the USA. The Sincerus Florida logo appears in teal and orange colors.*
FDA Label Image

Sdg (6102 2 Middle (inactives))

Sdg (6102 2 Middle (inactives))
Side label of the HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% product by Sincerus Florida, LLC, listing inactive ingredients such as Ascorbyl Palmitate FCC, Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning 1501 and 9011, Edetate Disodium USP Dihydrate, Kojic Acid, Purified Water USP, Sodium Chloride USP, Sodium Metabisulfite NF, and Vitamin E Acetate USP Liquid with their corresponding 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.