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: 0a35ac19-6883-a733-e063-6294a90ad22d
SPL ID: 262e192e-cfcc-6344-e063-6294a90af4c5
Version: 2
Effective date: 2024-11-05
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:34

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 · 15 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	68229-407-02	openfda.package_ndc
ndc	package	68229-407-03	openfda.package_ndc
ndc	package	68229-407-01	openfda.package_ndc
ndc	product	68229-407	openfda.product_ndc
ndc11	package	68229040702	derived:openfda.package_ndc
ndc11	package	68229040703	derived:openfda.package_ndc
ndc11	package	68229040701	derived:openfda.package_ndc
spl id		262e192e-cfcc-6344-e063-6294a90af4c5	id
spl set id		0a35ac19-6883-a733-e063-6294a90ad22d	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.