Hyaluronic Acid Sodium Salt 1% / Tacrolimus 0.1% / Urea 20%
Product Images NDC 72934-2097

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 1% / Tacrolimus 0.1% / Urea 20% (NDC 72934-2097). 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.

Product Images & Figures Index

FDA Label Image

Z (2 End)

Z (2 End)
A white plastic container showing a partial label of HYALURONIC ACID SODIUM SALT 1% / TACROLIMUS 0.1% / UREA 20% by Sincerus Florida, LLC. The visible text includes directions for use, storage instructions at controlled room temperature (20-25C), and contact information for Sincerus Florida, LLC in Pompano Beach, FL. There is also a small QR code on the label.*
FDA Label Image

Sxf (2097 2 Front)

Sxf (2097 2 Front)
Packaging label for HYALURONIC ACID SODIUM SALT 1% / TACROLIMUS MONOHYDRATE USP 0.1% / UREA USP 20% cream, 30 gm. The label includes the NDC 72934-2097-2 and states it is a compounded drug made in the USA. The labeler is Sincerus Florida, LLC, with their logo visible on the packaging.*
FDA Label Image

Ad (2097 2 Middle)

Ad (2097 2 Middle)
Label of HYALURONIC ACID SODIUM SALT 1% / TACROLIMUS 0.1% / UREA 20% cream by Sincerus Florida, LLC. The label lists active ingredients as Hyaluronic Acid Sodium Salt 1%, Tacrolimus Monohydrate USP 0.1%, and Urea USP 20%. It also shows inactive ingredients comprising 78.9% of the product. Additional details include a warning section and manufacturing and lot information.*

* 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.