141061 Hydrocortisone 0.5% / Hydroquinone 8% / Tretinoin 0.025%
Product Images NDC 72934-6233

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 141061 Hydrocortisone 0.5% / Hydroquinone 8% / Tretinoin 0.025% (NDC 72934-6233). 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

Ff (2 End)

Ff (2 End)
Directions for use panel on a white cylindrical container for 141061 HYDROCORTISONE 0.5% / HYDROQUINONE 8% / TRETINOIN 0.025% by Sincerus Florida, LLC. The panel includes instructions to use as directed by a physician, wash hands after use, apply topically, use externally only, and store at controlled room temperature. Manufacturer contact information and reporting guidance for adverse reactions are also provided.*
FDA Label Image

Er (6233 2 Front)

Er (6233 2 Front)
141061 Hydrocortisone 0.5% / Hydroquinone 8% / Tretinoin 0.025% emulsion in a white container. The label shows the NDC 72934-6233-2 and indicates the product is made by Sincerus Florida, LLC. The emulsion is packaged in a 30 gram container and is a compounded drug made in the USA.*
FDA Label Image

Xs (6233 2 Middle)

Xs (6233 2 Middle)
141061 HYDROCORTISONE 0.5% / HYDROQUINONE 8% / TRETINOIN 0.025% cream container showing the active and inactive ingredients label. Active ingredients include hydrocortisone USP 0.5%, hydroquinone USP 8%, tretinoin USP 0.025%. Inactive ingredients listed include citric acid USP anhydrous, cyclomethicone, Dow Corning 9011 and 1501, edetate disodium USP dihydrate, kojic acid, purified water USP, sodium chloride USP, and sodium metabisulfite NF. The label includes Rx only, lot number, BUD, and manufacturer details for Sincerus Florida, LLC.*

* 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.