FDA.reportPublic FDA data

Pain Relieving Patches

Manufacturer
Walgreen Company | Foshan Aqua Gel Biotech Co.,Ltd.
Effective date
2024-12-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:44:26

Label at a glance#

ProductPain Relieving Patches
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure11 sections

Storage and handling

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active IngredientPurpose
Camphor 1.2% Topical Analgesic
Menthol 5.7% Topical Analgesic
Methyl Salicylate 6.3% Topical Analgesic

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.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joins: arthritis, simple backache, muscle strains, muscle sprains and bruises.

WARNINGS

WARNINGS SECTION

For External Use Only

Allergy Alert:If prone to allergic reactions from aspirine or salicytates, consult a doctor before use.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years:

Clean and dry affected area. Remove patch from film, apply to affected area not more than 3-4 times a day.

Do not use for more than 8 hours.

Discard patch after use.

Children under 12 years of age, consult a physician.

Reseal pouch after opening.

PURPOSE

OTC - PURPOSE SECTION

Topical Analgesic

When using this product:

OTC - WHEN USING SECTION

  • Use only as directed
  • Avoid contact with eyes, mucous membranes or rashes.
  • DIspose of used patches away from children and pets. Used patches still contain the drug product which can produce serious adverse effects if children or pets chews or ingests the patch.

Do not use

OTC - DO NOT USE SECTION

  • On wounds or damaged skin
  • With a heating pad
  • If you are allergic to any ingredients in this product.
  • Otherwise then as directed.

top use and consult a doctor

OTC - STOP USE SECTION

  • If rash, itching or excessive skin irritation develops
  • If condition worsens
  • If symptoms last more than 7 days or clear up and occur again in a few days.

Storage and Care

STORAGE AND HANDLING SECTION

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

Pain Relieving Path

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DIST. BY
Walgreens Co.
200 Wilmot Rd
. Deerfield, IL 60015
www.walgreens.com

TOLL-FREE CUSTOMER CARE HELP LINE Mon–Fri, 8:30 am–4:30 pm CST 866-326-1313

Label Image
Label Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
853260camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated PatchPSN3
853260camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated PatchSCD3
853260camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated PatchSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9903-40Pain Relieving Patches40 in 1 BOXPATCH403
0363-9903-40Pain Relieving Patches9 g in 1 POUCHPATCH93

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-9903PAIN RELIEVING PATCHES (CAMPHOR MENTHOL METHYL SALICYTATE) PATCH [WALGREEN COMPANY]3Current NDC, Legacy NDC, 2 package rows20241220_13486792-d3d1-4585-beb7-24720b9edaae.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-99030363-9903-40

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
HYDROGENATED POLY(C6-14 OLEFIN; 2 CST)P0TX083987IACT
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)255PIF62MSIACT
LIQUID PETROLEUM6ZAE7X688JIACT
STYRENE44LJ2U959VIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB

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
Pain Relieving PatchesCAMPHOR MENTHOL METHYL SALICYTATEWalgreen Company13486792-d3d1-4585-beb7-24720b9edaae2024-12-18WarningsExact identifier
ndc (package): 0363-9903-40
ndc (product): 0363-9903
ndc11 (package): 00363990340
spl id: 298f80cb-2c7b-566a-e063-6394a90a91df
spl set id: 13486792-d3d1-4585-beb7-24720b9edaae

Reported adverse events (FAERS/openFDA)#

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