141011 Hydroquinone 6%
Product Images NDC 72934-6224

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 141011 Hydroquinone 6% (NDC 72934-6224). 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

Sd (2 End)

Sd (2 End)
Side label of 141011 HYDROQUINONE 6% topical product by Sincerus Florida, LLC showing directions for use. The label instructs to use as directed by a physician, apply topically, and wash hands after use. It includes contact information for Sincerus Florida, LLC in Pompano Beach, FL, and guidance to report adverse reactions to the FDA. It also states the product is for external and office use only, not for resale.*
FDA Label Image

Sdf (6224 2 Front)

Sdf (6224 2 Front)
141011 HYDROQUINONE 6% Emulsion in a white plastic container with a white cap. The label states the product contains 30 grams and features the Sincerus Florida logo. It is identified as a compounded drug made in the USA, with NDC 72934-6224-2 visible on the label.*
FDA Label Image

Asd (6224 2 Middle)

Asd (6224 2 Middle)
141011 HYDROQUINONE 6% topical emulsion bottle label showing active ingredient Hydroquinone USP 6%. The label listing includes inactive ingredients such as Citric Acid USP Anhydrous 0.2%, Cyclomethicone 10%, Dow Corning 1501 2%, Dow Corning 9011 0.25%, Edetate Disodium USP Dihydrate 0.12%, Kojic Acid 4%, Purified Water USP 64.85%, Sodium Chloride USP 0.5%, and Sodium Metabisulfite NF 0.2%. Product is labeled RX only and manufactured by 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.