Relief

Manufacturer
La Mend, Inc. | Akron Coating & Adhesives
Effective date
2024-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:17:11

Label at a glance#

ProductRelief
Active ingredientMENTHOL
Label structure9 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Dosage and administration

adults over 18 years: use one patch carefully remove the backing film and apply to the affected area no more than 3 to 4 times daily each patch can be worn up to 12 hours children under 18 years of age: consult a doctor

Storage and handling

store in a cool, dry place

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol (plant derived) 5%

Purpose

OTC - PURPOSE SECTION

Menthol (plant derived) 5%....................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product

  • use only as directed
  • avoid contact with the eyes and other mucous membranes
  • do not apply to wounds or damaged skin
  • do not bandage tightly
  • use only as directed

OTC - DO NOT USE SECTION

Do not use

  • more than one patch at a time
  • at the same time as other topical analgesics

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Posion Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults over 18 years:

  • use one patch
  • carefully remove the backing film and apply to the affected area no more than 3 to 4 times daily
  • each patch can be worn up to 12 hours
  • children under 18 years of age: consult a doctor

Other information

STORAGE AND HANDLING SECTION

  • store in a cool, dry place

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates Copolymer, Lavandula Angustifolia Oil, Arnica Montana Flower Extract, Aloe Barbadensis Leaf Extract, Eucalyptus Globulus Leaf Oil

Questions or Comments

OTC - QUESTIONS SECTION

(310) 909-8407 | thegoodpatch.com

You may also report serious side effects to this phone number

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The Good Patch

Relief

QTY. 04 PATCHES

Pain holding you back? Keep moving with this fast-acting, water-resistant topical patch. Made with plant-derived Menthol, Lavender, Arnica, and Aloe Vera.

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
420222menthol 5 % Medicated PatchPSN1
420222menthol 0.05 MG/MG Medicated PatchSCD1
420222menthol 5 % Medicated PatchSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72587-003-01Relief1 g in 1 PATCHPATCH11
72587-003-01Relief4 in 1 POUCHPATCH41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72587-003RELIEF (MENTHOL) PATCH [LA MEND, INC.]1Current NDC, 2 package rows20240815_1f92de3a-7180-5884-e063-6294a90aebf5.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72587-00372587-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
ReliefMENTHOLLa Mend, Inc.1f92de3a-7180-5884-e063-6294a90aebf52024-08-01WarningsExact identifier
ndc (package): 72587-003-01
ndc (product): 72587-003
ndc11 (package): 72587000301
spl id: 1f92de3a-7181-5884-e063-6294a90aebf5
spl set id: 1f92de3a-7180-5884-e063-6294a90aebf5

Reported adverse events (FAERS/openFDA)#

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