Lidocaine 5% Cream

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 5% Cream
Generic name: LIDOCAINE
Manufacturer: Medcore LLC
Product type: HUMAN OTC DRUG
SPL set ID: 15d02b42-bf8b-486a-a081-f6d17cc11ec7
SPL ID: 155520b3-0b6a-4267-a60e-8a1d3615a1c6
Version: 1
Effective date: 2026-05-07
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:43:59

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 5% Cream	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Medcore LLC	openfda.manufacturer_name
ndc	package	82461-420-30	openfda.package_ndc
ndc	product	82461-420	openfda.product_ndc
ndc11	package	82461042030	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		155520b3-0b6a-4267-a60e-8a1d3615a1c6	id
spl set id		15d02b42-bf8b-486a-a081-f6d17cc11ec7	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 eyes do not exceed recommended daily dosage unless directed by a physician do not put this product into the rectum by using fingers or any mechanical device or applicator. in case of bleeding, consult a doctor promptly

Reported adverse events (FAERS/openFDA)#

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