Benzocaine 20% / Lidocaine 10% / Tetracaine 10%
Product Images NDC 72934-2009

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 Benzocaine 20% / Lidocaine 10% / Tetracaine 10% (NDC 72934-2009). 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

Xf (2 End)

Xf (2 End)
Side view of a white container label for BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10% by Sincerus Florida, LLC. The label shows directions for use including application instructions, storage conditions, reporting safety information, and contact details for the manufacturer in Pompano Beach, Florida. A QR code is also visible on the label.*
FDA Label Image

X (2009 2 Front)

X (2009 2 Front)
Packaging label of BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10% cream in a 30 gram container. The label shows the NDC 72934-2009-2 and the manufacturer as Sincerus Florida, LLC. The product is labeled as a compounded drug made in the USA.*
FDA Label Image

Sd (2009 2 Middle)

Sd (2009 2 Middle)
Close-up image of a white container label showing the ingredient list of BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10% topical product by Sincerus Florida, LLC. The label details active ingredients benzocaine USP 20%, lidocaine USP 10%, and tetracaine USP 10%, along with inactive ingredients including butylated hydroxytoluene NF (BHT), cyclomethicone, dimethyl sulfoxide ACS, Dow Corning products, edetate disodium USP dihydrate, purified water USP, and salt stable lotion cream.*

* 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.