141016 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%
Product Images NDC 72934-6225

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for 141016 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025% (NDC 72934-6225). 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)

A text panel showing directions for use of 141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%, instructing to use as directed by a physician, apply topically, and wash hands after use. It states the product is for external use only, with storage recommended at controlled room temperature (20-25°C). The panel includes the labeler information: Sincerus Florida, LLC, Pompano Beach, FL with contact numbers and FDA reporting information.*

FDA Label Image

S (6225 2 Front)

141016 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025% emulsion in a white container. The label shows the product's active ingredients with their strengths, the NDC number 72934-6225-2, and a logo for Sincerus Florida, LLC. The packaging also notes it is a compounded drug made in the USA and lists the emulsion net weight as 30 gm.*

FDA Label Image

F (6225 2 Middle)

141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% in a white container with a label showing active and inactive ingredients. The label lists hydrocortisone USP 0.5%, hydroquinone USP 4%, tretinoin USP 0.025% as active ingredients and several inactive ingredients including citric acid USP anhydrous, cyclomethicone, and others. The product is labeled for Rx use and manufactured by 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.