Hydroquinone 8% / Tretinoin 0.025%
Product Images NDC 72934-6123

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% / Tretinoin 0.025% (NDC 72934-6123). 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

G (2 End)

G (2 End)
Close-up image of a white cylindrical container label showing partial usage directions and manufacturer contact information for a prescription product. The label mentions external use, washing hands after application, and storage at controlled room temperature. Sincerus Florida, LLC is listed as the labeler.*
FDA Label Image

F (6123 2 Front)

F (6123 2 Front)
Packaging label of HYDROQUINONE USP 8% / TRETINOIN USP 0.025% emulsion 30 gm by Sincerus Florida, LLC. The label includes the NDC number 72934-6123-2, the company logo, and states that it is a compounded drug made in the USA.*
FDA Label Image

C (6123 2 Middle)

C (6123 2 Middle)
Drug label active and inactive ingredients panel for HYDROQUINONE 8% / TRETINOIN 0.025% by Sincerus Florida, LLC. Active ingredients list hydroquinone USP 8% and tretinoin USP 0.025%. Inactive ingredients include citric acid USP anhydrous, cyclomethicone, Dow Corning 1501 and 9011, edetate disodium USP dihydrate, kojic acid, purified water USP, sodium chloride USP, and sodium metabisulfite NF with respective percentages.*

* 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.