Lidocaine 4 Percent

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 4 Percent
Generic name
LIDOCAINE
Manufacturer
ARI BRANDS, LLC
Product type
HUMAN OTC DRUG
SPL set ID
a6451b7d-20b9-46f5-84b3-5430cfe18219
SPL ID
a0cd961e-c7c7-446b-8ed6-41f6b9fa4a8a
Version
3
Effective date
2024-12-09
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:04:12
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 . Read all warnings and directions before use. Do not use • More than one patch at a time • On wounds or damaged skin • With a heating pad • If you are allergic to any ingredients of this product Allergy Alert: if you are allergic to any inactive ingredient of this product, contact a doctor before use. Whe n us ing this product • Use only as directed. • Avoid contact with eyes , mucous membranes, or rashes • Do not tightly wrap or bandage the treated area Stop use and as k a physician: • If pregnant or breast feeding • If localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling, and blistering • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. Keep out of reach of children and pets . If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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