Hydroquinone 4% / Tretinoin 0.025%
Product Images NDC 72934-6115

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 4% / Tretinoin 0.025% (NDC 72934-6115). 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

Sa (2 End)

Sa (2 End)
Side view of a white cylindrical container with a label showing directions for use and manufacturer information for HYDROQUINONE 4% / TRETINOIN 0.025% by Sincerus Florida, LLC. The label includes usage instructions, storage conditions, contact information, and a QR code.*
FDA Label Image

Ds (6115 2 Front)

Ds (6115 2 Front)
Packaging label of HYDROQUINONE USP 4% / TRETINOIN USP 0.025% emulsion, 30 gm, by Sincerus Florida. The label includes the NDC 72934-6115-2, states it is a compounded drug, and indicates it is made in the USA.*
FDA Label Image

Sf (6115 2 Middle)

Sf (6115 2 Middle)
Label panel of HYDROQUINONE 4% / TRETINOIN 0.025% showing active ingredients Hydroquinone USP 4% and Tretinoin USP 0.025%. The label lists inactive ingredients including Cyclomethicone, Citric Acid USP Anhydrous, Dow Corning 1501, Dow Corning 9011, Edetate Disodium USP Dihydrate, Kojic Acid, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF with their respective percentages. Also visible are the lot number and manufacturing and expiration 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.