Hyaluronic Acid Sodium Salt 0.5% / Niacinamide 4% / Tretinoin 0.05%
Product Images NDC 72934-2091

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 Hyaluronic Acid Sodium Salt 0.5% / Niacinamide 4% / Tretinoin 0.05% (NDC 72934-2091). 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

; (2091 2 End)

; (2091 2 End)
Label detail on a white plastic container for HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE 4% / TRETINOIN 0.05% by Sincerus Florida, LLC. Directions for use instruct application as directed by physician, use topically, wash hands after use, and store at controlled room temperature. Manufacturer contact details and FDA MedWatch reporting information are also visible.*
FDA Label Image

F (2091 2 Front)

F (2091 2 Front)
Packaging label of Hyaluronic Acid Sodium Salt 0.5% / Niacinamide 4% / Tretinoin 0.05% cream in a white cylindrical container. The label shows the NDC 72934-2091-2 and states the cream contains 30 grams. The labeler is Sincerus Florida, LLC, with a blue and orange Sincerus Florida logo. The label notes this is a compounded drug made in the USA.*
FDA Label Image

Hk (2091 2 Middle)

Hk (2091 2 Middle)
Bottle label for HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE 4% / TRETINOIN 0.05% cream by Sincerus Florida, LLC. The label lists active ingredients with their concentrations: Hyaluronic Acid Sodium Salt 0.5%, Niacinamide USP 4%, and Tretinoin USP 0.05%. It also includes inactive ingredients and manufacturing details.*

* 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.