Hyaluronic Acid Sodium Salt 0.5% / Niacinamide 4% / Tretinoin 0.025%
Product Images NDC 72934-2090

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 0.025% (NDC 72934-2090). 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

G (2090 2 End)

G (2090 2 End)
Side view of a white plastic container with a label showing directions for use and manufacturer contact information for HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE 4% / TRETINOIN 0.025% by Sincerus Florida, LLC. The label includes storage instructions, usage directions, and company address in Pompano Beach, FL.*
FDA Label Image

H (2090 2 Middle)

H (2090 2 Middle)
The image shows a white cylindrical container labeled for HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE 4% / TRETINOIN 0.025% cream. The label lists active ingredients with their respective concentrations and indicates the product is prescription only. Manufacturer details show it is labeled by Sincerus Florida, LLC. The lot number and manufacturing and expiration dates are partially visible.*
FDA Label Image

G (2090 2)

G (2090 2)
HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE USP 4% / TRETINOIN USP 0.025% cream in a 30gm container. The label shows NDC 72934-2090-2 and indicates the product is compounded by Sincerus Florida, LLC, made in the USA. The packaging is a white cylindrical container with the label featuring the Sincerus Florida logo in teal and orange.*

* 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.