Walgreens Flexible Pain Relieving Lidocaine Patch

Manufacturer
Walgreen Co.
Effective date
2024-11-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:40:34

Label at a glance#

ProductWalgreens Flexible Pain Relieving Lidocaine
Active ingredientLIDOCAINE
Label structure7 sections

Dosage and administration

Adults and children 12 years of age and over: Clean and dry affected area. Carefully remove backing from patch  Apply sticky side of patch to affected area  Use one patch for up to 8 hours Discard patch after single use Apply 1 patch at a time to affected area, not more than 3 to 4 times daily Children under 12 years of age:  consult a physician.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Use

INDICATIONS & USAGE SECTION

For temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Do not use 

OTC - DO NOT USE SECTION

  • More than one patch on your body at a time
  • On cut, irritated or swollen skin
  • On puncture wounds 
  • For more than one week without consulting a doctor
  • If you are allergic to any active or inactive ingredients
  • If pouch is damaged or opened

When using this product

OTC - WHEN USING SECTION

  • Use only as directed 
  • Read and follow all directions and warnings
  • Do not allow contact with the eyes
  • Do not use at the same time as other topical analgesics 
  • Do not bandage tightly or apply local heat (such as heating pads) to the area of use
  • Do not microwave
  • Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch

Stop use and consult a doctor if

OTC - STOP USE SECTION

  • Condition worsen
  • Redness is present
  • Irritation develops 
  • Symptoms persist for more than 7 days or clear up and occur again within a few days
  • You experience signs of skin injury, such as pain, swelling or blistering where the product was applied

If pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use. 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over:

  • Clean and dry affected area.
  • Carefully remove backing from patch 
  • Apply sticky side of patch to affected area 
  • Use one patch for up to 8 hours
  • Discard patch after single use
  • Apply 1 patch at a time to affected area, not more than 3 to 4 times daily

Children under 12 years of age: consult a physician.

Other information

SPL UNCLASSIFIED SECTION

  • Store in a clean, dry place outside of direct sunlight
  • Protect from excessive moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aluminum Silicate, Mineral Oil, Polyisobutylene, Propylene Glycol, Styrene-Isoprene-Styrene Block Copolymer, Terpene Resin.

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label..jpgLabel..jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737778lidocaine 4 % Medicated PatchPSN1
1737778lidocaine 0.04 MG/MG Medicated PatchSCD1
1737778lidocaine 4 % 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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-2182-01Walgreens Flexible Pain Relieving Lidocaine7 in 1 BOXPATCH71
0363-2182-01Walgreens Flexible Pain Relieving Lidocaine0.7 g in 1 POUCHPATCH0.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-2182WALGREENS FLEXIBLE PAIN RELIEVING LIDOCAINE (LIDOCAINE, MENTHOL) PATCH [WALGREEN CO.]1Current NDC, 2 package rows20241207_6f070fa3-a61a-4523-a470-ab58bf9400a3.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-21820363-2182-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
Walgreens Flexible Pain Relieving LidocaineLIDOCAINE, MENTHOLWalgreen Co.6f070fa3-a61a-4523-a470-ab58bf9400a32024-11-27WarningsExact identifier
ndc (package): 0363-2182-01
ndc (product): 0363-2182
ndc11 (package): 00363218201
spl id: 27eec6c5-dfef-ecc2-e063-6394a90af771
spl set id: 6f070fa3-a61a-4523-a470-ab58bf9400a3

Reported adverse events (FAERS/openFDA)#

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