Hydroquinone 8% / Tretinoin 0.025%.
Product Images NDC 72934-6124

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 Hydroquinone 8% / Tretinoin 0.025%. (NDC 72934-6124). 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

Swf (2 End)

Swf (2 End)
Label on a white cylindrical container for HYDROQUINONE 8% / TRETINOIN 0.025% by Sincerus Florida, LLC. The label includes directions for use, storage instructions, and contact information for the labeler in Pompano Beach, FL. A QR code is also visible on the label.*
FDA Label Image

Ds (6124 2 Front)

Ds (6124 2 Front)
Packaging label of HYDROQUINONE 8% / TRETINOIN 0.025% emulsion, 30 gm, from Sincerus Florida, LLC. The label prominently lists the active ingredients and their concentrations, includes the NDC 72934-6124-2, and states it is a compounded drug made in the USA. The label features the Sincerus Florida logo with teal and orange colors.*
FDA Label Image

Sdf (6124 2 Middle (inactives Only))

Sdf (6124 2 Middle (inactives Only))
Close-up of a white cylindrical container with a label listing inactive ingredients for HYDROQUINONE 8% / TRETINOIN 0.025%. The label details ingredients including 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. The label also contains usage directions partially visible on the side.*

* 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.