Hyaluronic Acid Sodium Salt 2% / Mometasone Furoate 0.1% / Niacinamide 4%
Product Images NDC 72934-2098

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 2% / Mometasone Furoate 0.1% / Niacinamide 4% (NDC 72934-2098). 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

B (2 End)

B (2 End)
Side view of a white plastic container with a label showing directions for use of a topical product by Sincerus Florida, LLC. Instructions include applying topically as directed by a physician and storage at controlled room temperature (20-25C). Contact information for Sincerus Florida in Pompano Beach, FL, and FDA reporting details are also visible, along with a QR code at the bottom.*
FDA Label Image

D (2098 2 Front)

D (2098 2 Front)
Packaging label of HYALURONIC ACID SODIUM SALT 2% / MOMETASONE FUROATE 0.1% / NIACINAMIDE 4% cream in a 30 gm container. The label shows the NDC 72934-2098-2 and identifies the product as a compounded drug made in the USA. The labeler is Sincerus Florida, LLC.*
FDA Label Image

S (2098 2 Middle)

S (2098 2 Middle)
Label on a white container for HYALURONIC ACID SODIUM SALT 2% / MOMETASONE FUROATE 0.1% / NIACINAMIDE 4% showing active ingredients and their concentrations, manufacturing and expiration dates, and partial labeler information. The label includes percentages for hyaluronic acid sodium salt, mometasone furoate USP, and niacinamide USP, along with inactive ingredients noted as a suspending cream.*

* 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.