LidoPatch Pain Relief

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
LidoPatch Pain Relief
Generic name
LIDOCAINE, MENTHOL
Manufacturer
JAR Laboratories
Product type
HUMAN OTC DRUG
SPL set ID
07289aa1-43ed-df31-e063-6394a90a764a
SPL ID
45112b5e-79d1-6fcd-e063-6394a90a87b5
Version
4
Effective date
2025-12-03
Source export date
2026-11-06
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:47:31
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use if you are allergic or sensitive to lidocaine or menthol. Do not reuse, apply to intact skin only. Do not use if pouch is damaged or opened. Handling and Disposal hands should be washed after the handling and eye contact should be avoided do not store patch outside the sealed pouch apply immediately after removal from protective pouch fold used patches so that the adhesive side sticks to itself and safely discard used patches or pieces of cut patches where children and pets cannot get them kept out of the reach of children both before and after use Stop use and ask a doctor if excessive redness or irritation is present condition worsens pain persists for more than 7 days symptoms clear up and occur again within a few days If pregnant or breast-feeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.