Medi-First Burn

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: Medi-First Burn
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 44bb5f25-1114-4bb1-8bcf-40402594abc4
SPL ID: 3e5d3698-aa18-ffc3-e063-6294a90a8227
Version: 9
Effective date: 2025-09-09
Source export date: 2026-10-27
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:23:15

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Medi-First Burn	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-477-69	openfda.package_ndc
ndc	product	47682-477	openfda.product_ndc
ndc11	package	47682047769	derived:openfda.package_ndc
rxcui		1011852	openfda.rxcui
spl id		3e5d3698-aa18-ffc3-e063-6294a90a8227	id
spl set id		44bb5f25-1114-4bb1-8bcf-40402594abc4	set_id
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 large quantities, particularly over raw or blistered areas When using this product avoid contact with the eyes Stop use ask a doctor if condition worsens symptoms persist for more than 7 days or clears up and occurs again within a few days Keep out of the 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.