Lidocaine 7% / Tetracaine 7%
Product Images NDC 72934-5142

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 7% / Tetracaine 7% (NDC 72934-5142). 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 (5142 4 End)

Sd (5142 4 End)
This is a white cylindrical container for LIDOCAINE 7% / TETRACAINE 7% by Sincerus Florida, LLC. The label on the container includes directions for use, advising application as directed by a physician and external use only, with storage instructions. The label also lists contact information for Sincerus Florida, LLC, including address and phone numbers, and a QR code is visible.*
FDA Label Image

Sf (5142 4 Front)

Sf (5142 4 Front)
LIDOCAINE 7% / TETRACAINE 7% ointment in a white cylindrical container labeled with the NDC 72934-5142-4. The label shows the active ingredients lidocaine USP 7% and tetracaine USP 7%, with a net content of 120 grams. Manufactured by Sincerus Florida, LLC, this is a compounded drug made in the USA.*
FDA Label Image

S (5142 4 Middle)

S (5142 4 Middle)
LIDOCAINE 7% / TETRACAINE 7% ointment in a white cylindrical container. The label lists the active ingredients as lidocaine USP and tetracaine USP, both at 7%, with inactive ingredient oleabase plasticized at 86%. The product is Rx only and 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.