Hydrocortisone 0.5% / Hydroquinone 8% / Tretinoin 0.05%
Product Images NDC 72934-6108

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 8% / Tretinoin 0.05% (NDC 72934-6108). 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

Asf (2 End)

Asf (2 End)
A label panel showing directions for use of a topical medication stating application instructions, storage conditions, and contact information for Sincerus Florida, LLC in Pompano Beach, FL. It includes a QR code and FDA contact numbers for reporting adverse reactions.*
FDA Label Image

Sdsg (6108 2 Front)

Sdsg (6108 2 Front)
Packaging label of HYDROCORTISONE 0.5% / HYDROQUINONE 8% / TRETINOIN 0.05% emulsion, 30gm, from Sincerus Florida, LLC. The label shows the product's active ingredients and strength with NDC 72934-6108-2 and indicates it is a compounded drug made in the USA.*
FDA Label Image

Asf (6108 2 Middle)

Asf (6108 2 Middle)
Label of HYDROCORTISONE 0.5% / HYDROQUINONE 8% / TRETINOIN 0.05% cream showing a list of active and inactive ingredients. Active ingredients include Hydrocortisone USP 0.5%, Hydroquinone USP 8%, and Tretinoin USP 0.05%. The label also lists inactive ingredients such as Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning 1501, Edetate Disodium USP Dihydrate, Emulsifix, Kojic Acid, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF. The labeler is Sincerus Florida, LLC.*

* 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.