Lidozen Gel

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 Gel
Generic name: LIDOCAINE HYDROCHLORIDE, MENTHOL
Manufacturer: Village Pharma LLC
Product type: HUMAN OTC DRUG
SPL set ID: ffb7831f-4ca9-4d73-8303-e9cd90078982
SPL ID: 43ca4fac-caaa-43e7-9c15-1ec8c69893d5
Version: 3
Effective date: 2026-01-01
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:57

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Lidozen Gel	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE, MENTHOL	openfda.generic_name
manufacturer name		Village Pharma LLC	openfda.manufacturer_name
ndc	package	71574-305-72	openfda.package_ndc
ndc	product	71574-305	openfda.product_ndc
ndc11	package	71574030572	derived:openfda.package_ndc
rxcui		1939340	openfda.rxcui
rxcui		1373137	openfda.rxcui
spl id		43ca4fac-caaa-43e7-9c15-1ec8c69893d5	id
spl set id		ffb7831f-4ca9-4d73-8303-e9cd90078982	set_id
unii		L7T10EIP3A	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. • 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.