FDA.reportPublic FDA data

Lorenza Pain Relief Patch

Manufacturer
Home Aide Diagnostics, Inc.
Effective date
2014-12-05
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:20:09

Label at a glance#

ProductLorenza Pain Relief Patch
Active ingredientLidocaine, Menthol
Label structure3 sections

Label contents#

Full prescribing information#

GENERAL PRECAUTIONS SECTION

This product may cause allergic reactions in some individuals.

DRUG FACTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DrugFacts.jpgDrugFacts.jpg

DESCRIPTION SECTION

LorenzaBox.jpgLorenzaBox.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1249758lidocaine 4 % / menthol 1 % Medicated PatchPSN1
1249758lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD1
1249758lidocaine 4 % / menthol 1 % Medicated PatchSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69379-014-172020-01-31C16284748780-19d75b9cf-d640-f424-e053-dadaa90a57ceLORENZA PAIN RELIEF PATCH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69379-014-17Lorenza Pain Relief Patch5 in 1 BOXPATCH51
69379-014-17Lorenza Pain Relief Patch3 in 1 PACKAGEPATCH31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69379-014LORENZA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]1Legacy NDC, 2 package rows20150116_0ca0aa7b-90f9-18b7-e054-00144ff8d46c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69379-014-17EA - Each69379-0147bfebedd-c8e5-4d27-a195-1fe3363993c012015-02-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
LidocaineACTIVE INGREDIENT98PI2009871
MentholACTIVE INGREDIENTL7T10EIP3A1
LidocaineACTIVE MOIETY98PI2009871
MentholACTIVE MOIETYL7T10EIP3A1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69379-01469379-014-17

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lidocaine98PI200987ACTIB
MentholL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0ca0aa7b-90fa-18b7-e054-00144ff8d46c0ca0aa7b-90f9-18b7-e054-00144ff8d46c2014-12-05Exact identifier
spl id: 0ca0aa7b-90fa-18b7-e054-00144ff8d46c
spl set id: 0ca0aa7b-90f9-18b7-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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