011021 Niacinamide 4% / Tretinoin 0.05%
Product Images NDC 72934-2204

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 011021 Niacinamide 4% / Tretinoin 0.05% (NDC 72934-2204). 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

X (2 End)

X (2 End)
The image shows the side label of a white plastic bottle for 011021 NIACINAMIDE 4% / TRETINOIN 0.05% by Sincerus Florida, LLC. The label includes directions for use, stating to apply topically as directed by a physician and wash hands after use. It also provides storage instructions and contact information for reporting adverse reactions.*
FDA Label Image

Gfh (2204 2 Front)

Gfh (2204 2 Front)
Bottle label for 011021 Niacinamide 4% / Tretinoin 0.05% cream, 30 gm, from Sincerus Florida, LLC. The label includes the NDC 72934-2204-2, indicates it is a compounded drug, and states it is made in the USA. The brand logo "Sincerus Florida" is visible on the label.*
FDA Label Image

Aqe (2204 2 Middle)

Aqe (2204 2 Middle)
The image shows a white cylindrical container with a label listing active and inactive ingredients. It includes Niacinamide USP 4% and Tretinoin USP 0.05% as active ingredients, with the remainder being a cream base. The product name 011021 NIACINAMIDE 4% / TRETINOIN 0.05% and labeler Sincerus Florida, LLC are partially visible.*

* 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.