Hydroquinone 6% / Tretinoin 0.05% / Triamcinolone 0.025%
Product Images NDC 72934-6120

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 6% / Tretinoin 0.05% / Triamcinolone 0.025% (NDC 72934-6120). 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

M (2 End)

M (2 End)
Label side of a white cylindrical container for HYDROQUINONE 6% / TRETINOIN 0.05% / TRIAMCINOLONE 0.025%, showing directions for use and manufacturer contact. Directions instruct to use as directed by a physician, apply topically, and store at controlled room temperature. Manufacturer is Sincerus Florida, LLC, Pompano Beach, FL. Includes phone numbers and a QR code on the label.*
FDA Label Image

C (6120 2 Front)

C (6120 2 Front)
HYDROQUINONE 6% / TRETINOIN 0.05% / TRIAMCINOLONE ACETONIDE 0.025% emulsion in a 30 gm container. The label includes the NDC 72934-6120-2 and shows the manufacturer as Sincerus Florida. The label also states this is a compounded drug made in the USA.*
FDA Label Image

J (6120 2 Middle)

J (6120 2 Middle)
Close-up of a white container showing the active and inactive ingredients label for HYDROQUINONE 6% / TRETINOIN 0.05% / TRIAMCINOLONE 0.025% from Sincerus Florida, LLC. The label lists active ingredients Hydroquinone USP 6%, Tretinoin USP 0.05%, and Triamcinolone Acetonide USP 0.025%, along with inactive ingredients such as Citric Acid USP Anhydrous and Cyclomethicone.*

* 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.