141060 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%
Product Images NDC 72934-6232

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 141060 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025% (NDC 72934-6232). 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

54 (2 End)

54 (2 End)
A white cylindrical container with a label displaying directions for use, storage instructions, and manufacturer contact information for Sincerus Florida, LLC. The label advises to apply topically as directed by a physician, use for external use only, wash hands after use, and store at controlled room temperature. Contact numbers and reporting information for adverse reactions are provided.*
FDA Label Image

Ad (6232 2 Front)

Ad (6232 2 Front)
141060 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% emulsion in a 30gm white bottle. The label includes the NDC number 72934-6232-2 and the Sincerus Florida, LLC logo in blue and orange. The product is identified as a compounded drug made in the USA.*
FDA Label Image

S (6232 2 Middle)

S (6232 2 Middle)
Close-up of a white bottle label showing the active and inactive ingredients for 141060 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% by Sincerus Florida, LLC. The label lists hydrocortisone USP, hydroquinone USP, and tretinoin USP as active ingredients, along with various inactive ingredients such as citric acid USP anhydrous, cyclomethicone, and sodium chloride USP.*

* 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.