Benzocaine 20% / Lidocaine 10% / Tetracaine 10%
Product Images NDC 72934-5009

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Benzocaine 20% / Lidocaine 10% / Tetracaine 10% (NDC 72934-5009). 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

Ad (2 End)

A side label panel showing the directions for use and manufacturer information for a Sincerus Florida, LLC product. It advises use as directed by a physician, topical application, external use only, washing hands after use, and storage at controlled room temperature (20-25°C). Contact information for reporting adverse reactions is also provided.*

FDA Label Image

Cc (5009 2 Front)

Packaging label of BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10% ointment, 30 grams, from Sincerus Florida, LLC. The label displays the active ingredients with their USP strengths, the National Drug Code 72934-5009-2, and states that it is a compounded drug made in the USA. The Sincerus Florida logo is also visible.*

FDA Label Image

Asd (5009 2 Middle)

Partial label of BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10% ointment showing active and inactive ingredients sections. Active ingredients listed include Benzocaine USP 20%, Lidocaine USP 10%, and Tetracaine USP 10%. Inactive ingredients include Butylated HydroxyToluene NF (BHT) 0.1% and Oleabase Plasticized 59.9%. Label also references prescription use and manufacturing and expiration dates.*

* 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.