LidoPro Patch (Lidocaine 4%, Menthol 1%)

LIDOCAINE AND MENTHOL PATCH TRANSDERMAL HUMAN OTC DRUG

LidoPro Patch (Lidocaine 4%, Menthol 1%) is an FDA drug label for the active ingredient LIDOCAINE AND MENTHOL PATCH manufactured by Clinic Pharma administered by TRANSDERMAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260728.

Generic name
LIDOCAINE AND MENTHOL PATCH
Manufacturer
Clinic Pharma
Product type
HUMAN OTC DRUG
Route
TRANSDERMAL
Dosage form
N/A
NDC
83881-402
Application
M017
Label effective
20260728

About this product

LidoPro Patch (Lidocaine 4%, Menthol 1%) is an FDA-registered drug product whose active ingredient is LIDOCAINE AND MENTHOL PATCH. It is labelled by Clinic Pharma taken by transdermal and marketed as a human otc drug product. Identifiers on file: NDC 83881-402, application M017, label effective 20260728. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing LIDOCAINE AND MENTHOL PATCH are most often described in connection with: temporary relief. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Lidocaine 4% Menthol 1%

Indications & Usage

Use For the temporary relief of pain

Dosage & Administration

Directions Adults 18 years and older: clean and dry the affected area open pouch and remove one patch remove protective film from patch apply one patch to the affected area of pain and leave in place for 8 to 12 hours if pain lasts after using the first patch, a second patch may be applied for up to another 8 to 12 hours only use one patch at a time wash hands with soap and water after applying or removing patch reseal pouch containing unused patches after each use

Warnings

Warnings For external use only Do not use on the face or rashes, on wounds or damaged skin in the eyes, mouth, or other mucous membranes on genitals with a heating pad right before or after heart surgery any patch from a pouch that has been opened for 7 or more days in large quantities, particularly over raw surfaces or blistered areas if tamper-evident seal is torn, broken, or missing more than 2 patches per day unless directed by a doctor children under 18 years of age Ask a doctor before use if you have allergies to topical products high blood pressure, heart disease, or kidney disease When using this product avoid contact with eyes. If eye contact occurs, rinse thoroughly with water the risk of heart attack or stroke may increase if you use more than directed or for longer than directed Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant of breastfeeding, ask a health professional before use Do not use during last 3 months of pregnancy because it may cause problems in the unborn child or complications during delivery. Keep out of reach of children. If ingested, seek medical help or contact a Poison Control Center 1-800-222-1222 right away. Dispose of the used patches by folding sticky ends together.

Frequently asked questions

What is LidoPro Patch (Lidocaine 4%, Menthol 1%) used for?
Use For the temporary relief of pain

Who makes LidoPro Patch (Lidocaine 4%, Menthol 1%)?
Clinic Pharma is the labeler of record for LidoPro Patch (Lidocaine 4%, Menthol 1%).

What form does LidoPro Patch (Lidocaine 4%, Menthol 1%) come in?
administered by transdermal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is LidoPro Patch (Lidocaine 4%, Menthol 1%) prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has LidoPro Patch (Lidocaine 4%, Menthol 1%) been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.