Burn with 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: Burn with Lidocaine
Generic name: BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 81363387-d4b1-4c3f-b67f-5017361c0fcd
SPL ID: 3e4ebe6a-8c81-0e41-e063-6394a90a5318
Version: 15
Effective date: 2025-09-08
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 06:05:00

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Burn with Lidocaine	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-260-99	openfda.package_ndc
ndc	package	47682-260-12	openfda.package_ndc
ndc	package	47682-260-73	openfda.package_ndc
ndc	product	47682-260	openfda.product_ndc
ndc11	package	47682026012	derived:openfda.package_ndc
ndc11	package	47682026099	derived:openfda.package_ndc
ndc11	package	47682026073	derived:openfda.package_ndc
rxcui		1012100	openfda.rxcui
spl id		3e4ebe6a-8c81-0e41-e063-6394a90a5318	id
spl set id		81363387-d4b1-4c3f-b67f-5017361c0fcd	set_id
unii		F5UM2KM3W7	openfda.unii
unii		V13007Z41A	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. Do not use in the eyes in large quantities over raw surfaces or blistered areas, or on deep puncture wounds, animal bites, or serious burns for more than 1 week unless directed by a doctor Stop use and ask doctor if the condition worsens or if symptoms persists for more than 7 days or clear up andoccur again within a few days Keep out of reach of children. If ingested, 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.