First Aid Only First Aid-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: First Aid Only First Aid-Burn
Generic name: BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Manufacturer: Acme United Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f31a44ff-e4ac-de1e-e053-2a95a90ab036
SPL ID: 2990220d-65fc-79b0-e063-6394a90a1736
Version: 4
Effective date: 2024-12-18
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:25:09

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		First Aid Only First Aid-Burn	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Acme United Corporation	openfda.manufacturer_name
ndc	package	0924-5702-00	openfda.package_ndc
ndc	package	0924-5702-02	openfda.package_ndc
ndc	package	0924-5702-05	openfda.package_ndc
ndc	package	0924-5702-07	openfda.package_ndc
ndc	package	0924-5702-04	openfda.package_ndc
ndc	package	0924-5702-03	openfda.package_ndc
ndc	package	0924-5702-01	openfda.package_ndc
ndc	package	0924-5702-06	openfda.package_ndc
ndc	product	0924-5702	openfda.product_ndc
ndc11	package	00924570205	derived:openfda.package_ndc
ndc11	package	00924570207	derived:openfda.package_ndc
ndc11	package	00924570206	derived:openfda.package_ndc
ndc11	package	00924570202	derived:openfda.package_ndc
ndc11	package	00924570200	derived:openfda.package_ndc
ndc11	package	00924570201	derived:openfda.package_ndc
ndc11	package	00924570204	derived:openfda.package_ndc
ndc11	package	00924570203	derived:openfda.package_ndc
rxcui		1012100	openfda.rxcui
spl id		2990220d-65fc-79b0-e063-6394a90a1736	id
spl set id		f31a44ff-e4ac-de1e-e053-2a95a90ab036	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 over large areas of the body in large quantities, particularly over raw surfaces or blistered areas if you are allergic to any of the ingredients on deep puncture wounds, animal bites, or serious burns more than one week unless directed by a doctor Keep out of reach of children . If swallowed contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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