Lidocaine Hydrochloride 2%

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 2%
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: Aldermed Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4977b722-d08d-3d9e-e063-6294a90a9035
SPL ID: 4aa8374e-199a-0e5b-e063-6394a90a0a94
Version: 3
Effective date: 2026-02-12
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:04

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Lidocaine Hydrochloride 2%	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Aldermed Inc.	openfda.manufacturer_name
ndc	package	87236-015-35	openfda.package_ndc
ndc	product	87236-015	openfda.product_ndc
ndc11	package	87236001535	derived:openfda.package_ndc
rxcui		1011852	openfda.rxcui
spl id		4aa8374e-199a-0e5b-e063-6394a90a0a94	id
spl set id		4977b722-d08d-3d9e-e063-6294a90a9035	set_id
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 Do not use ■ On wounds or damaged skin ■ In large quantities, particularly over raw surfaces or blistered areas When using this product ■ Avoid contact with the eyes ■ Do not bandage tightly Stop use and ask a doctor if ■ Condition worsens ■ Symptoms persist for more than 7 days ■ Symptoms clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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