LidoPro Patch

LIDOCAINE, MENTHOL, AND METHYL SALICYLATE TOPICAL HUMAN OTC DRUG

LidoPro Patch is an FDA drug label for the active ingredient LIDOCAINE, MENTHOL, AND METHYL SALICYLATE manufactured by Preferred Pharmaceuticals Inc. administered by TOPICAL. 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 20260521.

Generic name
LIDOCAINE, MENTHOL, AND METHYL SALICYLATE
Manufacturer
Preferred Pharmaceuticals Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
68788-8594
Application
M017
Label effective
20260521

About this product

LidoPro Patch is an FDA-registered drug product whose active ingredient is LIDOCAINE, MENTHOL, AND METHYL SALICYLATE. It is labelled by Preferred Pharmaceuticals Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 68788-8594, application M017, label effective 20260521. 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, MENTHOL, AND METHYL SALICYLATE are most often described in connection with: temporarily relieves, minor pain. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Lidocaine 4%Active Ingredient Menthol .5%Active Ingredient Methyl Salicylate .1%

Indications & Usage

Uses Temporarily relieves minor pain

Dosage & Administration

DIRECTIONS adults and children over 12 years: • clean and dry the affected area • remove patch from plastic liner and place on the affected area • use 1 patch for up to 12 hours • place used patch on the liner when not in use • re-use the patch up to 2 times. children 12 years or younger: ask a doctor

Warnings

Warnings For external use only Do not use • more than one patch on your bidy at a time or on cuts, irritated, or swollen skin • on puncture wounds • for more than one week without consulting a doctor. When using this product • Use only as directed. Read and follow directions and warning on this packaging. • Do not apply to wounds or damaged, broken, or irritated skin • Avoid contact with the eyes or mucous membranes • Do not bandage tightly or apply local heat (such as heating pads) to area of use • Do not use at the same time as other topical analgesics • Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch. Stop use and ask a doctor if • conditions worsens • redness is present • irritation develops • symptoms persist for more than 7 days or clear up and occur again within a few days • you experience signs of injury, such as pain, swelling, or blistering where the product was applied If pregnant or breast feeding, ask health professional before use. Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.

Frequently asked questions

What is LidoPro Patch used for?
Uses Temporarily relieves minor pain

Who makes LidoPro Patch?
Preferred Pharmaceuticals Inc. is the labeler of record for LidoPro Patch.

What form does LidoPro Patch come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is LidoPro Patch 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 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.