Hydroquinone 4%
Product Images NDC 72934-6114

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydroquinone 4% (NDC 72934-6114). 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

C (6114 2 End)

Label on a white cylindrical container for HYDROQUINONE 4%, by Sincerus Florida, LLC. The visible label section includes directions for use, advising application as directed by a physician, topical use, hand washing instructions, and storage at controlled room temperature. It also provides the labeler's address and contact information, as well as reporting instructions for adverse reactions.*

FDA Label Image

C (6114 2 Front)

The image shows a white airless pump bottle labeled HYDROQUINONE USP 4% Emulsion 30gm. The label includes the NDC number 72934-6114-2 and indicates it is a compounded drug made in the USA. It features a colored logo with the words SINCERUS and FLORIDA, the labeler of the product.*

FDA Label Image

X (6114 2 Middle)

A text panel listing the active and inactive ingredients for HYDROQUINONE 4% topical product by Sincerus Florida, LLC. The active ingredient is Hydroquinone USP at 4%. Inactive ingredients include Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning 1501, Dow Corning 9011, Edetate Disodium USP Dihydrate, Kojic Acid, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF, each with specific percentages or descriptions indicated.*

* 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.