Re-Lieved 3 in 1 Patch

Manufacturer
Transfer Technology | Transfer Technoloy | Akron Coating & Adhesive
Effective date
2025-01-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:52:23

Label at a glance#

ProductRe-Lieved 3 in 1 Patch
Active ingredientMENTHOL, (+)-, CAMPHOR (SYNTHETIC), METHYL SALICYLATE
Label structure13 sections

Dosage and administration

Clean and dry affected area remove patch from film apply to affected area not more than 3 to 4 times daily remove patch from the skin afer a maximum of 8 hours application

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.1%

Menthol 6.0%

Methyl Salicylate 10.0%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

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

  • arthritis
  • strains
  • simple backache
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only.

Allergy alert: If prone to allergic reaction from asirin or salicylates, consult a doctor before use

Do not use

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • if you are allergic to any ingredients of this product

When using this product

OTC - WHEN USING SECTION

  • Use only as directed
  • avoid contact with the eyes, mucous membranes or rashes
  • so ot bandage tightly

Stop use or ask a doctor if

OTC - STOP USE SECTION

  • rash, itching, or excessive skin irritation develops
  • Condition worsens
  • Symptoms persist for more than 7 days
  • Symptoms clear up and occur again within a few days

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. Store new and dispose of used product out of reach of children.

Directions adults/children 12 years or older

DOSAGE & ADMINISTRATION SECTION

  • Clean and dry affected area
  • remove patch from film
  • apply to affected area not more than 3 to 4 times daily
  • remove patch from the skin afer a maximum of 8 hours application

Other information

OTHER SAFETY INFORMATION

  • avoid storing product in dirct sunlight
  • protect product from excessive moisture

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Polyethylene, Acrylic adhesive

Re-Lieved 3 in 1 Patch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3 in 1 Patch3 in 1 Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71662-003-60Re-Lieved 3 in 1 Patch19 mg in 1 POUCHPATCH192

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71662-003RE-LIEVED 3 IN 1 PATCH (MENTHOL, CAMPHOR, METHYL SALICYLATE PATCH) PATCH [TRANSFER TECHNOLOGY]2Current NDC, Legacy NDC, 1 package rows20250112_e9ab9a03-b9e3-7317-e053-2995a90a9950.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
71662-00371662-003-60

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
Re-Lieved 3 in 1 PatchMENTHOL, CAMPHOR, METHYL SALICYLATE PATCHTransfer Technologye9ab9a03-b9e3-7317-e053-2995a90a99502025-01-11WarningsExact identifier
ndc (package): 71662-003-60
ndc (product): 71662-003
ndc11 (package): 71662000360
spl id: 2b743728-1f2c-4ba8-e063-6294a90a74a2
spl set id: e9ab9a03-b9e3-7317-e053-2995a90a9950

Reported adverse events (FAERS/openFDA)#

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