Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%
Product Images NDC 72934-6100

3 FDA label images from Sincerus Florda, 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 72934-6100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florda, 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

Sd (2 End)

Sd (2 End)
The image shows a white cylindrical container with a partial view of the label. The label includes directions for use stating application is as directed by a physician, topical use only, hand washing after use, and storage at controlled room temperature (20-25C). The label lists the manufacturer as Sincerus Florida, LLC, Pompano Beach, FL, with contact numbers and a QR code.*
FDA Label Image

Sdf (6100 2 Front)

Sdf (6100 2 Front)
Packaging label of HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% emulsion, 30 gm, by Sincerus Florida, LLC. The label displays the NDC 72934-6100-2 and states the product is a compounded drug made in the USA. The label features the Sincerus Florida logo with teal and orange colors.*
FDA Label Image

Asdf (6100 2 Middle)

Asdf (6100 2 Middle)
Close-up of a white cylindrical container label for HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% by Sincerus Florda, LLC. The label lists active ingredients with concentrations and multiple inactive ingredients including citric acid USP anhydrous, cyclomethicone, and kojic acid among others.*

* 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.