Lidozen

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: Lidozen
Generic name: LIDOCAINE, MENTHOL
Manufacturer: Proficient Rx LP
Product type: HUMAN OTC DRUG
SPL set ID: 488d665c-a4fe-4a69-bab3-34b2347f4b05
SPL ID: f687fe54-1e59-45c2-859f-cb3279ed259d
Version: 6
Effective date: 2023-12-01
Source export date: 2026-11-06
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:46:01

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Lidozen	openfda.brand_name
generic name		LIDOCAINE, MENTHOL	openfda.generic_name
manufacturer name		Proficient Rx LP	openfda.manufacturer_name
ndc	package	71205-348-15	openfda.package_ndc
ndc	package	71205-348-30	openfda.package_ndc
ndc	package	71205-348-05	openfda.package_ndc
ndc	product	71205-348	openfda.product_ndc
ndc11	package	71205034815	derived:openfda.package_ndc
ndc11	package	71205034805	derived:openfda.package_ndc
ndc11	package	71205034830	derived:openfda.package_ndc
rxcui		1249758	openfda.rxcui
rxcui		2201504	openfda.rxcui
spl id		f687fe54-1e59-45c2-859f-cb3279ed259d	id
spl set id		488d665c-a4fe-4a69-bab3-34b2347f4b05	set_id
unii		98PI200987	openfda.unii
unii		L7T10EIP3A	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. • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. Do not use • in large quantities, particularly over raw surfaces or blistered areas. If pregnant or breast-feeding, ask a health professional before use. Keep out of 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.