Hydroquinone 8%
Product Images NDC 72934-6121

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 8% (NDC 72934-6121). 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

X (6121 2 Front)

X (6121 2 Front)
Label of HYDROQUINONE USP 8% emulsion 30gm by Sincerus Florida, LLC shows the NDC 72934-6121-2. The label indicates it is a compounded drug made in the USA with the Sincerus Florida logo in teal and orange.*
FDA Label Image

D (6121 2 End)

D (6121 2 End)
HYDROQUINONE 8% in a white cylindrical container with a label showing directions for use, manufacturer details, and contact information for Sincerus Florida, LLC. The label instructs external use only and storage at controlled room temperature (20-25C).*
FDA Label Image

S (6121 2 Middle)

S (6121 2 Middle)
Label on a cylindrical container for HYDROQUINONE 8% topical product by Sincerus Florida, LLC. The label lists active ingredient Hydroquinone USP at 8% and inactive ingredients including Citric Acid USP, Cyclomethicone, Dow Corning 1501 and 9011, Edetate Disodium USP Dihydrate, Kojic Acid, Purified Water USP, Sodium Chloride USP, and Sodium Metabisulfite NF with corresponding percentages. The label also displays Rx only and manufacturing and lot details.*

* 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.