Lidocaine Patch
Product Images NDC 63629-8755

3 FDA label images from Bryant Ranch Prepack · 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 63629-8755). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chemical Structure For Lidocaine (Image 1)

Chemical Structure For Lidocaine (Image 1)
Chemical structure of Lidocaine, showing its molecular formula with aromatic rings, amide, and tertiary amine groups as part of its composition.*
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). (Image 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). (Image 2)
A line graph showing plasma lidocaine concentration (ng/mL) measured over a 72-hour period. The x-axis represents time in hours, and the y-axis represents plasma lidocaine levels. The graph illustrates multiple peaks and troughs of lidocaine concentrations over time.*
FDA Label Image

Label (Lbl636298755)

Label (Lbl636298755)
Lidocaine Patch 5% topical patch label by Bryant Ranch Prepack, containing 30 patches. The label indicates each adhesive patch contains lidocaine 700 mg (50 mg per gram) in an aqueous base. It includes storage instructions and a warning to keep patches out of reach of children and pets.*

* 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.