Lidocaine Hydrochloride

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: Lidocaine Hydrochloride
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: YYBA CORP
Product type: HUMAN OTC DRUG
SPL set ID: 582a0001-da1e-909a-e063-6394a90a2b11
SPL ID: 582a0001-da1f-909a-e063-6394a90a2b11
Version: 1
Effective date: 2026-08-03
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:19

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		M015	openfda.application_number
brand name		Lidocaine Hydrochloride	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		YYBA CORP	openfda.manufacturer_name
ndc	package	73581-120-06	openfda.package_ndc
ndc	package	73581-120-02	openfda.package_ndc
ndc	package	73581-120-01	openfda.package_ndc
ndc	product	73581-120	openfda.product_ndc
ndc11	package	73581012002	derived:openfda.package_ndc
ndc11	package	73581012006	derived:openfda.package_ndc
ndc11	package	73581012001	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		582a0001-da1f-909a-e063-6394a90a2b11	id
spl set id		582a0001-da1e-909a-e063-6394a90a2b11	set_id
unii		98PI200987	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. When using this product avoid contact with etes do not use in large quantities, particulary over large surfaces or blistered areas do not exceed recommended dosage unless directed by a doctor do not put this product into the rectum by using fingers or any mechanical device or applicator

Reported adverse events (FAERS/openFDA)#

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