Lidocaine 23% / Tetracaine 7%
Product Images NDC 72934-5140

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 Lidocaine 23% / Tetracaine 7% (NDC 72934-5140). 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

Zc (5140 4 End)

Zc (5140 4 End)
A white cylindrical container with a small rectangular label containing text instructions. The product is Lidocaine 23% / Tetracaine 7% from Sincerus Florida, LLC. The label includes directions for use, storage conditions, and contact information for the manufacturer located in Pompano Beach, FL. No dosage form or package size is visible on the container.*
FDA Label Image

Zc (5140 4 Front)

Zc (5140 4 Front)
Packaging label of Lidocaine USP 23% and Tetracaine USP 7% ointment in a white cylindrical container. The label displays NDC 72934-5140-4, states the product weight as 120 grams, and features the Sincerus Florida logo. Text indicates it is a compounded drug made in the USA.*
FDA Label Image

Da (5140 4 Middle)

Da (5140 4 Middle)
LIDOCAINE 23% / TETRACAINE 7% ointment in a white cylindrical container with a label showing active ingredients Lidocaine USP 23% and Tetracaine USP 7%, along with inactive ingredients including Butylated Hydroxytoluene NF (BHT) and Oleabase Plasticized. The label includes manufacturing dates and lot number details. 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.