Lidocaine 23% / Tetracaine 7%
Product Images NDC 72934-2140

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 72934-2140). 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

Q (2 End)

Q (2 End)
Side label of a LIDOCAINE 23% / TETRACAINE 7% product container by Sincerus Florida, LLC. The label includes directions for use, advising application as directed by a physician and storage at controlled room temperature. Contact information for Sincerus Florida, LLC in Pompano Beach, FL, and FDA reporting details are also visible. The container is white with black text and a QR code at the bottom of the label.*
FDA Label Image

Ad (2140 2 Front)

Ad (2140 2 Front)
Packaging label of LIDOCAINE 23% / TETRACAINE 7% cream in a 30gm container. The label includes the NDC number 72934-2140-2 and states the product is a compounded drug made in the USA by Sincerus Florida, LLC.*
FDA Label Image

2140 2 Ingredients

2140 2 Ingredients
LIDOCAINE 23% / TETRACAINE 7% cream in a white plastic container. The label shows active ingredients Lidocaine USP 23% and Tetracaine USP 7%, along with inactive ingredients including Butylated Hydroxytoluene NF, Dimethyl Sulfoxide ACS, Lipobase Heavy, Pluronic Gel 30%, and Polysorbate 80 NF. The product is labeled for Rx only with a lot number and BUD date, manufactured 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.