LidoPro

LidoPro is an FDA-registered drug product whose active ingredient is LIDOCAINE AND MENTHOL. It is labelled by Clinic Pharma taken by transdermal and marketed as a human otc drug product. Identifiers on file: NDC 83881-403, application M017, label effective 20260728. It is one of 19 FDA drug label records sharing the active ingredient LIDOCAINE AND MENTHOL. 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.

Across FDA labelling, products containing LIDOCAINE AND MENTHOL 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.

Use Temporarily relieves minor pain

Directions Adults and children 12 years of age and over: clean and dry affected area, free of lotions, ointments, and creams. Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Do not use more than one patch in a 12-hour period. Maximum 2 patches per day. Discard patch after single use. Children under 12 years of age: consult a physician.

Warnings For external use only Do not use more than one patch on your body at a time on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor if you are allergic to any active or inactive ingredients if pouch is damaged or opened When using this use only as directed read and follow all directions and warnings on this carton do not allow contact with the eyes do not use at the same time as other topical analgesics do not bandage tightly or apply local heat (such as heating pads) to the area of use do not microwave 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 consult a doctor if condition 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 skin injury, such as pain, swelling, or blistering where the product was applied If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center 1-800-222-1222 right away.

FDA lists 19 drug label records with LIDOCAINE AND MENTHOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is LidoPro used for?
Use Temporarily relieves minor pain

Who makes LidoPro?
Clinic Pharma is the labeler of record for LidoPro. 19 FDA label records share the active ingredient LIDOCAINE AND MENTHOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does LidoPro 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 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.

Are there other products containing LIDOCAINE AND MENTHOL?
Yes. 19 FDA drug label records list LIDOCAINE AND MENTHOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has LidoPro been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.