Drugplain

LidoPro Patch (Lidocaine 4%, Menthol 1%) 336 mg/8400mg

Lidocaine and Menthol Patch · PATCH · Advanced Rx of Tennessee, LLC

No Recall HistoryCurrently in Shortage
Plain English

LidoPro Patch (Lidocaine 4%, Menthol 1%) is a patch containing lidocaine and menthol patch at 336 mg/8400mg, taken transdermal. Manufactured by Advanced Rx of Tennessee, LLC.

Key Facts

Brand Name
LidoPro Patch (Lidocaine 4%, Menthol 1%)
Generic Name
Lidocaine and Menthol Patch
NDC Code (Product)
80425-0506
Manufacturer
Advanced Rx of Tennessee, LLC
Strength
336 mg/8400mg
Dosage Form
PATCH
Route
TRANSDERMAL
Marketing Status
Application #
M017
Drug Class
Amide Local Anesthetic [EPC]; Antiarrhythmic [EPC]
Marketing Start
03/20/2025

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses For the temporary relief of pain.

Dosage & Administration

Directions Adults 18 years and older: • clean and dry 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

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 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 breast-feeding, 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…

Frequently Asked Questions

What is LidoPro Patch (Lidocaine 4%, Menthol 1%) used for?

LidoPro Patch (Lidocaine 4%, Menthol 1%) contains Lidocaine and Menthol Patch. It is a patch taken transdermal. Consult your doctor for specific uses.

Is LidoPro Patch (Lidocaine 4%, Menthol 1%) a controlled substance?

LidoPro Patch (Lidocaine 4%, Menthol 1%) is not classified as a controlled substance by the DEA.

What is the generic name for LidoPro Patch (Lidocaine 4%, Menthol 1%)?

The generic name for LidoPro Patch (Lidocaine 4%, Menthol 1%) is Lidocaine and Menthol Patch. There are no other listed brand versions of Lidocaine and Menthol Patch.

What is the NDC code for LidoPro Patch (Lidocaine 4%, Menthol 1%) 336 mg/8400mg?

The NDC (National Drug Code) for LidoPro Patch (Lidocaine 4%, Menthol 1%) 336 mg/8400mg is 80425-0506, listed by Advanced Rx of Tennessee, LLC.

Product NDC

80425-0506

Package NDC

80425-0506-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)