Lidocaine 5% Patch
Product Images NDC 60760-657

3 FDA label images from St. Mary's Medical Park Pharmacy · 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 5% (NDC 60760-657). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

Molecule (Molecule)

Molecule (Molecule)
Chemical structure of lidocaine showing its molecular arrangement including aromatic ring with two methyl groups, amide linkage, and diethylaminoethyl side chain.*
FDA Label Image

Graphs (Graphs)

Graphs (Graphs)
A plasma concentration-time graph showing plasma lidocaine levels (ng/mL) on the Y-axis over a 72-hour period on the X-axis. The graph displays three cyclical peaks of plasma lidocaine concentration, with levels rising and falling periodically across the 72-hour timeframe.*
FDA Label Image

657-05 (Lidocaine 60760 657 05)

657-05 (Lidocaine 60760 657 05)
Lidocaine 5% Patch packaging label showing the product name, strength, and dosage form as a topical patch. The label indicates a quantity of 5 patches per package, with space for lot number, expiration date, and RX number, which are not filled in. It displays the NDC code 60760-657-05 and states the product is manufactured by Allergan Italia Srl in Avellino, Italy, and packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. The label includes usage instructions to use as directed, storage temperature range, and regulatory symbols including a barcode and a QR code.*

* 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.