141055 Hydroquinone 6%
Product Images NDC 72934-6230

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 141055 Hydroquinone 6% (NDC 72934-6230). 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

Fd (2 End)

Fd (2 End)
The image shows a drug label panel with directions for use and manufacturer contact information. It instructs to use as directed by a physician, apply topically, and store at controlled room temperature (20-25C). The label lists Sincerus Florida, LLC in Pompano Beach, FL, along with a phone number and FDA contact information for reporting adverse reactions. It states the product is for office use only and not for resale.*
FDA Label Image

5 (6230 2 Front)

5 (6230 2 Front)
141055 HYDROQUINONE 6% Emulsion 30gm in a white container with a label showing the product name, strength, and dosage form. The label includes the NDC 72934-6230-2 and the Sincerus Florida logo. It specifies that this is a compounded drug made in the USA.*
FDA Label Image

S (6230 2 Middle)

S (6230 2 Middle)
141055 HYDROQUINONE 6% packaging label from Sincerus Florida, LLC shows a cylindrical container with a white label listing active ingredient hydroquinone USP 6% and multiple inactive ingredients including citric acid USP anhydrous, cyclomethicone, Dow Corning 1501, Dow Corning 9011, edetate disodium USP dihydrate, emulsifix, hyaluronic acid sodium salt, krisgel 100, purified water USP, sodium chloride USP, and sodium metabisulfite NF.*

* 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.