Lidothol Gel
Product Images NDC 87063-218

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lidothol (NDC 87063-218). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa 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

Package Insert (1) (Lidothol Package Insert 102424 01 (1))

This is a drug information panel for Lidothol gel containing Lidocaine HCl 4.5% and Menthol 5%. It includes dosage and administration instructions, handling and disposal guidelines, overdose information, adverse reactions, examples of drugs associated with methemoglobinemia, and clinical pharmacology details. The panel also features the product logo and manufacturer information from Clinic Pharma.*

FDA Label Image

Package Insert (2) (Lidothol Package Insert 102424 02 (1))

This text panel provides detailed prescribing information for Lidothol gel, including sections on distribution, metabolism, excretion, indication and usage, contraindications, warnings, precautions, allergic reactions, and drug interactions. It also covers special population considerations such as pregnancy, nursing mothers, pediatric use, and safety information related to methemoglobinemia and local anesthetics. The information is organized in multiple columns for clarity.*

FDA Label Image

1 (Label)

The Lidothol gel packaging label shows it contains Lidocaine HCl and Menthol at a 5 g/100g strength in a 3.5 oz tube. The label includes the NDC 87063-218-99, batch number, expiration date, and indicates the product is manufactured for Clinic Pharma by Enovachem Pharmaceuticals. It also lists storage instructions and cautions for dispensing without prescription.*

* 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.