Active Ingredient
Lidocaine 4%
Menthol .5%
Methyl Salicylate .1%
The following Structured Product Label (SPL) was submitted to the FDA by Advanced Rx Pharmacy Of Tennessee, Llc for the product Lidopro Patch (NDC 80425-0374). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, if pregnant orbreast feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine 4%
Menthol .5%
Methyl Salicylate .1%
Topical Anesthetic
Topical Analgesic
Topical Counterirritant
Temporarily relieves minor pain
For external use only
• 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.
ask health professional before use.
If swallowed, get medical help or contact a Poison Control Center right away.
adults and children over 12 years:
children 12 years or younger: ask a doctor
Distributed by
Advanced Rx Pharmacy of Tennessee, LLC
Vegan Glycerol, Polyacrylate, Aqua. Polysorbate 80
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