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 Burn
Generic name: BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Manufacturer: Water-Jel Technologies
Product type: HUMAN OTC DRUG
SPL set ID: 25ebf112-8ac3-4402-9a87-00e454ab7efa
SPL ID: 5f3a0aa8-f1a3-6d47-e053-2a91aa0a77fa
Version: 5
Effective date: 2017-11-30
Source export date: 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:17:02

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		part348	openfda.application_number
brand name		First Aid Burn	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Water-Jel Technologies	openfda.manufacturer_name
ndc	package	59898-902-03	openfda.package_ndc
ndc	package	59898-902-01	openfda.package_ndc
ndc	package	59898-902-36	openfda.package_ndc
ndc	package	59898-902-02	openfda.package_ndc
ndc	product	59898-902	openfda.product_ndc
ndc11	package	59898090236	derived:openfda.package_ndc
ndc11	package	59898090202	derived:openfda.package_ndc
ndc11	package	59898090203	derived:openfda.package_ndc
ndc11	package	59898090201	derived:openfda.package_ndc
rxcui		1012100	openfda.rxcui
spl id		5f3a0aa8-f1a3-6d47-e053-2a91aa0a77fa	id
spl set id		25ebf112-8ac3-4402-9a87-00e454ab7efa	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 or apply over large areas of the body longer than 1 week unless directed by a doctor in large quantities, particularly over raw surfaces or blistered areas Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns When using this product avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days condition 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.