Pentoxifylline 0.5% / Triamcinolone Acetonide 0.1%
Product Images NDC 72934-1169

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 Pentoxifylline 0.5% / Triamcinolone Acetonide 0.1% (NDC 72934-1169). 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

S (2 End)

S (2 End)
Side view of a white container label for PENTOXIFYLLINE 0.5% / TRIAMCINOLONE ACETONIDE 0.1% by Sincerus Florida, LLC. The label includes usage directions: apply topically as directed by a physician, for external use only, wash hands after use, and storage at controlled room temperature (20-25C). Manufacturer contact information and a QR code are also visible.*
FDA Label Image

X (1169 2 Front)

X (1169 2 Front)
The image shows a white container labeled with PENTOXIFYLLINE USP 0.5% and TRIAMCINOLONE ACETONIDE USP 0.1% gel, 30 gm. The label includes the NDC number 72934-1169-2 and the logo for Sincerus Florida, LLC. The product is noted as a compounded drug and made in the USA.*
FDA Label Image

X (1169 2 Middle)

X (1169 2 Middle)
Label of PENTOXIFYLLINE 0.5% / TRIAMCINOLONE ACETONIDE 0.1% gel showing active ingredients Pentoxifylline USP 0.5% and Triamcinolone Acetonide USP 0.1%, along with inactive ingredients silicone gel, in a 30 gram tube. The label includes manufacturing and expiration dates and states Rx only. The product is labeled by Sincerus Florida, LLC.*

* 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.