Hydroquinone 6%
Product Images NDC 72934-6118

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% (NDC 72934-6118). 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

E (6118 2 End)

E (6118 2 End)
The image shows a white cylindrical container with a label containing use directions and manufacturer information for HYDROQUINONE 6% by Sincerus Florida, LLC. The label includes instructions to apply topically as directed by a physician, store at controlled room temperature, and contact information for reporting adverse reactions. A QR code is also visible on the label.*
FDA Label Image

Z (6118 2 Front)

Z (6118 2 Front)
The image shows a white bottle label for HYDROQUINONE 6% Emulsion USP, 30 gm, produced by Sincerus Florida, LLC. The label includes the NDC number 72934-6118-2 and states that this is a compounded drug made in the USA. The label prominently features the Sincerus Florida logo in teal and orange colors.*
FDA Label Image

E (6118 2 Middle)

E (6118 2 Middle)
Label on a white container for HYDROQUINONE 6%, distributed by Sincerus Florida, LLC. The label lists active ingredient Hydroquinone USP 6% and several inactive ingredients including Citric Acid USP Anhydrous, Cyclomethicone, and Dow Corning products among others. It includes batch details with a lot number and manufacturing date.*

* 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.