Hydrocortisone 1% / Hydroquinone 8% / Tretinoin 0.05%
Product Images NDC 72934-6109

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 Hydrocortisone 1% / Hydroquinone 8% / Tretinoin 0.05% (NDC 72934-6109). 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

Sf (2 End)

Sf (2 End)
Label on a white cylindrical container with directions for use stating application as directed by a physician, topical use only, and to store at controlled room temperature (20-25°C). The label includes contact information for Sincerus Florida, LLC, located in Pompano Beach, FL, with phone numbers for reporting suspected adverse reactions and a QR code.*
FDA Label Image

As (6109 2 Front)

As (6109 2 Front)
Container label for HYDROCORTISONE 1%, HYDROQUINONE 8%, TRETINOIN 0.05% emulsion, 30 grams, manufactured by Sincerus Florida, LLC. The label includes the NDC number 72934-6109-2, compound drug designation, and a colorful Sincerus Florida logo.*
FDA Label Image

H (6109 2 Middle)

H (6109 2 Middle)
A white cylindrical container displaying a label listing active and inactive ingredients for HYDROCORTISONE 1% / HYDROQUINONE 8% / TRETINOIN 0.05%, by Sincerus Florida, LLC. The label details percentages of ingredients, including Hydrocortisone USP 1%, Hydroquinone USP 8%, and Tretinoin USP 0.05%, along with inactive ingredients such as Citric Acid USP Anhydrous, Cyclomethicone, and others.*

* 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.