Lidoderm
Product Images NDC 21695-075

3 FDA label images from Rebel Distributors Corp. · 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 Lidoderm (NDC 21695-075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp., 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

Package Label (075)

Package Label (075)
Lidoderm 5% Patch #30 packaging label shows it contains lidocaine 700mg per patch (50mg per gram adhesive). The label states it is for prescription use only, with methylparaben and propylparaben as preservatives. The manufacturer is Teikoku Seiyaku Co., Ltd., and the packager is Physician Partner, Thousand Oaks, CA.*
FDA Label Image

Lidocaine Structure (Lidoderm 1)

Lidocaine Structure (Lidoderm 1)
Chemical structure diagram of the active ingredient in LIDODERM, showing a molecule containing a benzene ring with two methyl groups and an amide-linked ethylamino side chain.*
FDA Label Image

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

Figure 1mean Lidocaine Blood Concentrations After Three Consecutive Daily Applications Of Three Lidoderm Patches Simultaneously For 12 Hours Per Day In Healthy Volunteers (n = 15). (Lidoderm 2)
A line graph depicting plasma lidocaine concentration in ng/mL over time in hours, showing cyclic peaks approximately every 24 hours across 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.