Pain and Itch Relief 4% Lidocaine

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: Pain and Itch Relief 4% Lidocaine
Generic name: LIDOCAINE
Manufacturer: Walgreens
Product type: HUMAN OTC DRUG
SPL set ID: f84e76a9-6af6-4fd1-be4e-efa05728cbfd
SPL ID: bf04ac41-f6f2-4539-ae51-5d5a99dc8216
Version: 4
Effective date: 2025-12-09
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 03:10:55

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Pain and Itch Relief 4% Lidocaine	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Walgreens	openfda.manufacturer_name
ndc	package	0363-3001-24	openfda.package_ndc
ndc	product	0363-3001	openfda.product_ndc
ndc11	package	00363300124	derived:openfda.package_ndc
spl id		bf04ac41-f6f2-4539-ae51-5d5a99dc8216	id
spl set id		f84e76a9-6af6-4fd1-be4e-efa05728cbfd	set_id
unii		98PI200987	openfda.unii

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. Avoid contact with eyes. Not for prolonged use. Do not use in large quantities, particularly over raw surfaces or blistered areas. Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occurs again within a few days rash or irritation develops, persists, or increases If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Reported adverse events (FAERS/openFDA)#

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