FDA.reportPublic FDA data

Walgreens Kinesiology Pain Relief

Manufacturer
Walgreen Co.
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:45:16

Label at a glance#

ProductWalgreens Kinesiology Pain Relief
Active ingredientLIDOCAINE, MENTHOL
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 starting at a corner Apply sticky side of patch to affected area  Discard after single use Children under 12 years of age:  consult a physician.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Topical analgesic

Use

INDICATIONS & USAGE SECTION

For temporary relief of pain

Warning

WARNINGS SECTION

For external use only

Do not use 

OTC - DO NOT USE SECTION

  • 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

When using this product

OTC - WHEN USING SECTION

  • Use only as directed 
  • Apply only to clean dry and untreated skin
  • 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 worsens
  • 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 breastfeeding, 

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use. 

Keep out of reach of children and pets.

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 starting at a corner
  • Apply sticky side of patch to affected area 
  • Discard after single use

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 Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1249758lidocaine 4 % / menthol 1 % Medicated PatchPSN2
1249758lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD2
1249758lidocaine 4 % / menthol 1 % Medicated PatchSY2

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
0363-9657-00Walgreens Kinesiology Pain Relief20 in 1 BOXTAPE202
0363-9657-00Walgreens Kinesiology Pain Relief1250 mg in 1 APPLICATORTAPE12502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-9657WALGREENS KINESIOLOGY PAIN RELIEF (LIDOCAINE, MENTHOL) TAPE [WALGREEN CO.]2Current NDC, 2 package rows20241222_0fdbb310-8e65-4e0c-b413-a093964324a2.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-96570363-9657-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM SILICATET1FAD4SS2MIACT
MINERAL OILT5L8T28FGPIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMERK7S96QM8DVIACT
TERPENE RESINGR35AH6YDNIACT
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
Walgreens Kinesiology Pain ReliefLIDOCAINE, MENTHOLWalgreen Co.0fdbb310-8e65-4e0c-b413-a093964324a22024-12-19WarningsExact identifier
ndc (package): 0363-9657-00
ndc (product): 0363-9657
ndc11 (package): 00363965700
spl id: 29a68f7b-c375-ff3c-e063-6394a90aca24
spl set id: 0fdbb310-8e65-4e0c-b413-a093964324a2

Reported adverse events (FAERS/openFDA)#

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