Lidocaine 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
Lidocaine Pain Relief
Generic name
LIDOCAINE PAIN RELIEF
Manufacturer
PAI Holdings, LLC dba PAI Pharma
Product type
HUMAN OTC DRUG
SPL set ID
963978de-8295-47ee-9b06-64c3521aa994
SPL ID
096b4296-4123-4481-af04-4caa75e381a0
Version
8
Effective date
2026-02-26
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:11:47
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 more than one patch at a time on wounds or damaged, broken or irritated skin if you are allergic to any ingredients of this product When using this product use only as directed • read and follow all directions and warnings do not allow contact with eyes and mucous membranes do not bandage tightly • do not apply local heat such as a heating pad do not use other topical anesthetics at the same time Stop use and ask a doctor if localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering conditions worsen symptoms persist for more than 7 days symptoms clear up and occur again within a few days if pregnant or breast-feeding, ask a healthcare professional before use. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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