QC Burn Relief Aloe

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: QC Burn Relief Aloe
Generic name: LIDOCAINE HCL
Manufacturer: Chain Drug Marketing Association Inc
Product type: HUMAN OTC DRUG
SPL set ID: b5e76f0c-0bfe-b13e-e053-2995a90a0861
SPL ID: 295784a9-db52-649d-e063-6294a90a6a4b
Version: 3
Effective date: 2024-12-15
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:33:03

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		M017	openfda.application_number
brand name		QC Burn Relief Aloe	openfda.brand_name
generic name		LIDOCAINE HCL	openfda.generic_name
manufacturer name		Chain Drug Marketing Association Inc	openfda.manufacturer_name
ndc	package	63868-095-08	openfda.package_ndc
ndc	product	63868-095	openfda.product_ndc
ndc11	package	63868009508	derived:openfda.package_ndc
rxcui		1011849	openfda.rxcui
spl id		295784a9-db52-649d-e063-6294a90a6a4b	id
spl set id		b5e76f0c-0bfe-b13e-e053-2995a90a0861	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

For external use only . Do not use in large quantities, particularly over raw surfaces or blistered areas. When using this product avoid contact with eyes. Rinse with water if contact occurs. Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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