Lidocaine Cream
Product Images NDC 10135-672

2 FDA label images from Marlex Pharmaceuticals Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Lidocaine (NDC 10135-672). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex Pharmaceuticals Inc, 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

Principal Display Panel (15g Tube CartonLidocaine 4% Topical Anesthetic CreamPain & Itch Relief Cream NET WT. 0.5 oz.(15g))

Principal Display Panel (15g Tube CartonLidocaine 4% Topical Anesthetic CreamPain & Itch Relief Cream NET WT. 0.5 oz.(15g))
Label for Lidocaine 4% Topical Anesthetic Cream by Marlex Pharmaceuticals, Inc. The cream contains 4% lidocaine and is packaged in a 15-gram container. The label includes Drug Facts with active ingredient, uses, warnings, directions, other information, and inactive ingredients. The product is for external topical use only.*
FDA Label Image

Principal Display Panel (30g Tube CartonLidocaine 4% Topical Anesthetic CreamPain & Itch Relief Cream NET WT. (30g))

Principal Display Panel (30g Tube CartonLidocaine 4% Topical Anesthetic CreamPain & Itch Relief Cream NET WT. (30g))
Packaging label for Lidocaine 4% Topical Anesthetic Cream by Marlex Pharmaceuticals Inc. The label indicates a 30 gram tube with 4% lidocaine concentration. It includes drug facts detailing the active ingredient, uses for minor skin conditions, warnings, directions for use, other storage information, and a list of inactive ingredients. The label is intended for external use only.*

* 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.