Alocane Plus

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: Alocane Plus
Generic name: LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE
Manufacturer: Quest Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 24538037-1d74-48a0-b909-98ecc57651fe
SPL ID: 3a24dd33-2000-ccc2-e063-6394a90a8f13
Version: 10
Effective date: 2025-07-17
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 06:28:05

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Alocane Plus	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Quest Products, Inc.	openfda.manufacturer_name
ndc	package	68229-300-01	openfda.package_ndc
ndc	package	68229-300-03	openfda.package_ndc
ndc	package	68229-300-02	openfda.package_ndc
ndc	package	68229-300-04	openfda.package_ndc
ndc	product	68229-300	openfda.product_ndc
ndc11	package	68229030002	derived:openfda.package_ndc
ndc11	package	68229030001	derived:openfda.package_ndc
ndc11	package	68229030004	derived:openfda.package_ndc
ndc11	package	68229030003	derived:openfda.package_ndc
rxcui		2587646	openfda.rxcui
rxcui		2375042	openfda.rxcui
spl id		3a24dd33-2000-ccc2-e063-6394a90a8f13	id
spl set id		24538037-1d74-48a0-b909-98ecc57651fe	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. Avoid contact with eyes. Keep out of reach of children. Stop use and ask doctor: if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding , ask a health care professional before use.

Reported adverse events (FAERS/openFDA)#

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