Lidocaine
Product Images NDC 50436-1330

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 50436-1330). 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

Label Image (Lbl504361330)

Label Image (Lbl504361330)
Lidocaine Patch 5% packaging label from Unit Dose Services, containing 30 patches. The label indicates the product is manufactured by Watson Labs, Inc., Salt Lake City, Utah. It includes storage instructions, manufacturer details, and placeholders for lot number and expiration date. The NDC number is 50436-1330-1.*
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 functional groups including aromatic ring, amide linkage, and ethylamine side chains.*
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 (hours). The graph shows multiple peaks and troughs, indicating cyclic variations in plasma lidocaine levels up to 72 hours.*

* 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.