Lidocaine
Product Images NDC 45865-912

3 FDA label images from Medsource Pharmaceuticals · 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 (NDC 45865-912). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medsource Pharmaceuticals, 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

Pdp (912)

Pdp (912)
Lidocaine transdermal patch 5% in a 30 patch per box package labeled as generic for Lidoderm, manufactured by Actavis Labs UT, Inc. The label specifies external use only and advises application to affected areas as directed by a physician. The patch is rectangular and white.*
FDA Label Image

Chemical Structure For Lidocaine (Lidocaine Patch 1)

Chemical Structure For Lidocaine (Lidocaine Patch 1)
Chemical structure diagram of lidocaine showing its molecular formula with labeled atomic groups including methyl, amide linkage, and ethyl amine substituents.*
FDA Label Image

Figure 1 Mean Lidocaine Blood Concentrations After Three Consecutive Daily Applications Of Three Lidocaine Patches Simultaneously For 12 Hours Per Day In Healthy Volunteers (n = 15). (Lidocaine Patch 2)

Figure 1 Mean Lidocaine Blood Concentrations After Three Consecutive Daily Applications Of Three Lidocaine Patches Simultaneously For 12 Hours Per Day In Healthy Volunteers (n = 15). (Lidocaine Patch 2)
A line graph depicting plasma lidocaine concentration (ng/mL) over time in hours, showing three repeated peaks approximately 18 hours apart, indicating fluctuating plasma levels of lidocaine over a 72-hour period.*

* 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.