Alocane Max

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 Max
Generic name: LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE
Manufacturer: Quest Products LLC
Product type: HUMAN OTC DRUG
SPL set ID: 0a33f9a9-1fdc-7cdf-e063-6294a90adca1
SPL ID: 4de08098-5946-ba6e-e063-6294a90a8dbe
Version: 7
Effective date: 2026-03-25
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 06:28:15

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 · 33 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Alocane Max	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Quest Products LLC	openfda.manufacturer_name
ndc	package	68229-406-01	openfda.package_ndc
ndc	package	68229-406-02	openfda.package_ndc
ndc	package	68229-406-08	openfda.package_ndc
ndc	package	68229-406-09	openfda.package_ndc
ndc	package	68229-406-11	openfda.package_ndc
ndc	package	68229-406-85	openfda.package_ndc
ndc	package	68229-406-03	openfda.package_ndc
ndc	package	68229-406-07	openfda.package_ndc
ndc	package	68229-406-06	openfda.package_ndc
ndc	package	68229-406-10	openfda.package_ndc
ndc	package	68229-406-05	openfda.package_ndc
ndc	product	68229-406	openfda.product_ndc
ndc11	package	68229040608	derived:openfda.package_ndc
ndc11	package	68229040602	derived:openfda.package_ndc
ndc11	package	68229040685	derived:openfda.package_ndc
ndc11	package	68229040601	derived:openfda.package_ndc
ndc11	package	68229040605	derived:openfda.package_ndc
ndc11	package	68229040606	derived:openfda.package_ndc
ndc11	package	68229040603	derived:openfda.package_ndc
ndc11	package	68229040609	derived:openfda.package_ndc
ndc11	package	68229040611	derived:openfda.package_ndc
ndc11	package	68229040610	derived:openfda.package_ndc
ndc11	package	68229040607	derived:openfda.package_ndc
rxcui		2587646	openfda.rxcui
rxcui		2375042	openfda.rxcui
spl id		4de08098-5946-ba6e-e063-6294a90a8dbe	id
spl set id		0a33f9a9-1fdc-7cdf-e063-6294a90adca1	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. Ask a doctor before use if you have: Deep or puncture wounds Animal bites Serious burns Do not use: In or near the eyes In large quantities or over large areas of the body On raw surfaces or blistered areas 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. Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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