Hydroquinone 5% / Tretinoin 0.025% / Triamcinolone Acetonide 0.025%
Product Images NDC 72934-6117

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 5% / Tretinoin 0.025% / Triamcinolone Acetonide 0.025% (NDC 72934-6117). 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

Fs (2 End)

Fs (2 End)
Side view of a white cylindrical container with a label showing directions for use and manufacturer information. The text mentions application instructions and contact details for Sincerus Florida, LLC, the labeler of HYDROQUINONE 5% / TRETINOIN 0.025% / TRIAMCINOLONE ACETONIDE 0.025%. A QR code is visible at the bottom of the label.*
FDA Label Image

Sf (6117 2 Front)

Sf (6117 2 Front)
The image shows a white cylindrical bottle labeled with the product HYDROQUINONE USP 5%, TRETINOIN USP 0.025%, TRIAMCINOLONE ACETONIDE USP 0.025% emulsion, 30 gm. The label includes the NDC number 72934-6117-2 and displays the Sincerus Florida logo with text indicating it is a compounded drug made in the USA.*
FDA Label Image

Ss (6117 2 Middle)

Ss (6117 2 Middle)
Label of HYDROQUINONE 5% / TRETINOIN 0.025% / TRIAMCINOLONE ACETONIDE 0.025% showing active and inactive ingredients. Active ingredients include Hydroquinone USP 5%, Tretinoin USP 0.025%, and Triamcinolone Acetonide USP 0.025%. Inactive ingredients are listed with their percentages, including Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning compounds, Edetate Disodium USP Dihydrate, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF. The label also indicates the labeler as 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.