Relief

Manufacturer
La Mend, Inc.
Effective date
2024-10-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:52:24

Label at a glance#

ProductRelief
Active ingredientMENTHOL
Label structure13 sections

Storage and handling

store in a cool, dry place

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol (plant derived) 5%

OTC - PURPOSE SECTION

Topical Analgesic

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

  • 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

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

OTC - STOP USE SECTION

  • 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

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

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

STORAGE AND HANDLING SECTION

  • store in a cool, dry place

INACTIVE INGREDIENT SECTION

methyl acrylate, 2-ethylhexyl acrylate, acrylic acid copolymer, hydroxyethyl acrylate, vinyl acetate copolymer, lavender oil, arnica montana extract, aloe vera extract, eucalyptus oil

OTC - QUESTIONS SECTION

(310) 909-8407 | thegoodpatch.com

You may also report serious side effects to this phone number

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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.

ReliefRelief

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72587-002-012024-01-30C16284748780-11030e365-4383-111a-e063-dadaa90a10e2Relief

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
72587-00272587-002-01

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
2-ETHYLHEXYL ACRYLATEHR49R9S6XGIACT
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
2486990a-25f0-8c2e-e063-6394a90ac5fcda84cf2f-d7a3-698e-e053-2995a90a52d32024-10-15WarningsExact identifier
spl id: 2486990a-25f0-8c2e-e063-6394a90ac5fc
spl set id: da84cf2f-d7a3-698e-e053-2995a90a52d3

Reported adverse events (FAERS/openFDA)#

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