Lidocaine Patch
Product Images NDC 0591-2679

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocaine (NDC 0591-2679). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Actavis Pharma, Inc., 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

Lidocaine Patch Novaplus A200675 1

Lidocaine Patch Novaplus A200675 1
Chemical structure diagram showing the molecular formula of Lidocaine, the active ingredient in this product. The diagram illustrates the arrangement of carbon, hydrogen, nitrogen, and oxygen atoms in Lidocaine's molecular structure.*
FDA Label Image

Lidocaine Patch Novaplus A200675 2

Lidocaine Patch Novaplus A200675 2
A line graph depicting plasma lidocaine concentration (ng/mL) over time (hours) up to 72 hours. The graph shows multiple peaks and troughs, indicating fluctuating plasma levels of lidocaine across the time course.*
FDA Label Image

Lidocaine Patch Novaplus A200675 3

FDA Label Image

Lidocaine Patch Novaplus A200675 4

Lidocaine Patch Novaplus A200675 4
The image shows a flat layout of the carton packaging for Lidocaine Patch 5% by Actavis Pharma, Inc. The front panel highlights the product name, strength, and active ingredient quantity per patch (700 mg lidocaine). It notes 30 patches in 30 envelopes, each containing 1 patch. The packaging also includes inactive ingredients, usage directions, warnings to keep out of reach from children and pets, and application instructions with diagrams. The Novaplus+ logo is present on the carton.*

* 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.