Ndc 72934- 5010-4 Benzocaine 20% / Lidocaine 8% / Tetracaine 4%.
Product Images NDC 72934-5010

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ndc 72934- 5010-4 Benzocaine 20% / Lidocaine 8% / Tetracaine 4%. (NDC 72934-5010). 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

Sd (5010 4 End)

Bottle label of NDC 72934-5010-4 BENZOCAINE 20% / LIDOCAINE 8% / TETRACAINE 4% topical product by Sincerus Florida, LLC. The label provides directions for use, advising application as directed by a physician, for external use only, and to wash hands after use. It includes storage instructions and manufacturer contact information.*

FDA Label Image

Cs (5010 4 Front)

The image shows a white cylindrical container labeled as NDC 72934-5010-4 Benzoaine 20%, Lidocaine 8%, Tetracaine 4% ointment, 120 gm. The label includes the brand name Sincerus Florida and states that this is a compounded drug made in the USA. Additional information about lot and manufacturing date is partially visible on the side label.*

FDA Label Image

Sd (5010 4 Middle)

A white cylindrical container labeled as NDC 72934-5010-4 BENZOCAINE 20% / LIDOCAINE 8% / TETRACAINE 4% ointment. The visible label includes a table listing active ingredients benzocaine, lidocaine, and tetracaine with their respective concentrations, as well as inactive ingredients butylated hydroxytoluene, blue water, and oleabase plastcrized. The labeler is 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.