Lidocaine
Product Images NDC 50436-3525

3 FDA label images from Unit Dose Services · 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 50436-3525). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Chemical Structure For Lidocaine (Image 1)

Chemical Structure For Lidocaine (Image 1)
Chemical structure diagram of Lidocaine showing its molecular configuration with aromatic ring, amide linkage, and diethylamino group.*
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 depicting plasma lidocaine concentration (ng/mL) over time (hours) spanning 0 to 72 hours. The graph shows multiple peaks and troughs indicating fluctuating plasma lidocaine levels across the time course.*
FDA Label Image

Label Image (Lbl504363525)

Label Image (Lbl504363525)
Lidocaine Patch 5%, package containing 30 patches, manufactured by Actavis Labs UT, Inc. in Salt Lake City, UT. Each patch contains 700 mg lidocaine (50 mg per gram adhesive). The label includes storage instructions, product codes, and a note that it is for prescription use only, labeled by Unit Dose Services, LLC, Florida.*

* 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.