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Lidenza Patch Package Insert

Status:
Prescription (Rx) Facts
Strength:
4 g/100 g, 1 g/100 g
Active ingredients:

Prescribing information (package insert) - Lidenza Patch

Warnings

For external use only

Avoid contact with eyes

Do not applly to open wounds or damaged skin

If symptoms persist for more than seven days, discontinue use and consult physician

If swallowed, consult physician

Do not bandage tightly

If pregnant or breast feeding, contact physician prior to use

Do not use in large quantities, particularly over raw surfaces or blistered areas

Keep out of reach of children

Lidocaine HCL 4.00%

Menthol 1.00%

aloe barbadensis leaf, water, arnica montan extract, boswella serrata extract, camelia sinensis leaf extract, carbomer, ethylhexylglycerine, glycerine, isopropyl myristate, PEG 8, phenoxyethanol, polysorbate 80, sodium lauryl sulfate, triethanolamine, fd&c blue #1, fd&c yellow #5

clean and dry affected area

remove patch from backing and apply to affected area

use only one patch at a time, and maximum of four patches/day

leave patch on affected area for up to 8 hours

do not use patches for longer than five consecutive days

children under 12 should consult physician prior to use

Temporary relief of pain associated with minor cuts, scrapes and minor skin irritations

Topical anesthetic

External analgesic

About this document

Source: FDA drug labeling via NLM DailyMed · View the label on DailyMed

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Drug information for Lidenza Patch

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Amide Local Anesthetic, Antiarrhythmic
Active ingredients Lidocaine hydrochloride 4 g/100 g, Menthol 1 g/100 g
Dosage form Patch
Route Topical
Marketing status not in the current FDA NDC Directory
Company (applicant) Patchwerx Labs, Inc.
FDA approval UNAPPROVED DRUG OTHERUnapproved drug
Packages (NDC)
Package
4 g/100 g, 1 g/100 g – 100 g in 1 package NDC 69329-017-15
4 g/100 g, 1 g/100 g – 100 g in 1 package NDC 69329-017-25

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.