Hydroquinone 6% /tretinoin 0.05%
Product Images NDC 72934-6119

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% (NDC 72934-6119). 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

C (2 End)

C (2 End)
This image shows the side panel of a white cylindrical container for HYDROQUINONE 6% / TRETINOIN 0.05% topical product by Sincerus Florida, LLC. The label includes directions for use, contact information for the labeler, and a QR code. The directions state to use as directed by a physician, apply topically, for external use only, with storage at controlled room temperature.*
FDA Label Image

D (6119 2 Front)

D (6119 2 Front)
The image shows a white cylindrical container labeled as HYDROQUINONE USP 6% and TRETINOIN USP 0.05% emulsion, 30 grams. The label includes the NDC number 72934-6119-2 and displays the logo of Sincerus Florida. It notes that this is a compounded drug, made in USA.*
FDA Label Image

M (6119 2 Middle)

M (6119 2 Middle)
Side label of HYDROQUINONE 6% / TRETINOIN 0.05% showing active ingredients Hydroquinone USP 6% and Tretinoin USP 0.05%, with a list of inactive ingredients including Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning compounds, Edetate Disodium USP Dihydrate, Kojic Acid, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF with their respective percentages. The label also displays manufacturing and beyond-use dates.*

* 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.