Active Ingredient
Lidocaine 4%
The following Structured Product Label (SPL) was submitted to the FDA by Velocity Pharma Llc for the product Maximum Strength Lidocaine Patch (NDC 76168-067). 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 or breast feeding, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine 4%
Topical Anesthetic
Temporarily relieves minor pain
For external use only
ask a 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
aluminium hydroxide gel, bentonite, borax, carbomer, carboxymethylcellulose sodium,
colloidal silicon dioxide, dihydroxyaluminumaminoacetate, disodiumedetate, gelatin, glycerin, oleic acid, polysorbate 80, polyvinyl Alcohol, potassium Sorbate, povidone, propylene glycol, sodiummetabisulphite, tartaric acid, trolamine, urea, water
MAX STRENGTH LIDOCAINE PATCH
-NUMBS AWAY PAIN
* Please review the disclaimer below.