FDA.reportPublic FDA data

Re-Lieved Lidocaine Patch

Manufacturer
Transfer Technology | Transfer Technoloy
Effective date
2024-10-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:42:08

Label at a glance#

ProductRe-Lieved Lidocaine Patch
Active ingredientMENTHOL, (+)-, LIDOCAINE
Label structure14 sections

Dosage and administration

Clean and dry affected area Peel patch off plastic liner and place on affected area for no more than 12 hours Wash hands after applying patch. Under age 12, consult a physician before use For easier removal of the patc, apply rubbing alcohol or baby oil to adhesive edge while gently peeling

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

For the temporary relief of pain.

Warnings

WARNINGS SECTION

For external use only.The adhesoin properties of this patch may cause an extended period of redness. Please visit www.re-lieved.com for more information.

Do not use

OTC - DO NOT USE SECTION

If you are allergic to Lidocaine. On open wounds or on damaged, broken or irritated skin. Remove immidiately if you sense a burning sensation after application.

When using this product

OTC - WHEN USING SECTION

  • Do not use other topical products
  • Do not allow contact with eyes or mucous membranes
  • Keep away from excessive heat. Do not apply heating pad to area of use
  • Apply only to clean, dry and untreated skin
  • Use only as directed. Read and follow all directions and warnings on this label

Ask your doctor or pharmacist before use if you are

OTC - ASK DOCTOR SECTION

using blood thinning medication, steroids, or non-steroidal anti-inflammatory druns (NSAIDs), or if you have sensitive skin.

Stop use or ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • Symptoms persist for more than 7 days

If pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a physician before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If put in mouth, get medical help or contact a poison control center right away. Dispose of used product away from children and pets.

Directionsadults/children 12 years or older

DOSAGE & ADMINISTRATION SECTION

  • Clean and dry affected area
  • Peel patch off plastic liner and place on affected area for no more than 12 hours
  • Wash hands after applying patch.
  • Under age 12, consult a physician before use
  • For easier removal of the patc, apply rubbing alcohol or baby oil to adhesive edge while gently peeling

Other information

OTHER SAFETY INFORMATION

  • store at room termperature
  • Do not exceed 100 oFahrenheit, 38 oCelsius

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylic adhesive, Polyethylene fabric

Re-Lieved Lidocaine-Menthol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Re-Lieved Lidocaine plus MentholRe-Lieved Lidocaine plus Menthol

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 Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71662-001-06Re-Lieved Lidocaine Patch5 mg in 1 POUCHPATCH52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71662-001RE-LIEVED LIDOCAINE PATCH (LIDOCAINE PATCH 4%) PATCH [TRANSFER TECHNOLOGY]2Legacy NDC, 1 package rows20241212_ba5cd48c-cd43-2f63-e053-2a95a90a930f.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
71662-00171662-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S)1PEZ3NLY6IIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
MENTHOL, (+)-C6B1OE8P3WACTIB
LIDOCAINE98PI200987ACTIB

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
24b27c05-e17d-083d-e063-6394a90a0fe7ba5cd48c-cd43-2f63-e053-2a95a90a930f2024-10-17WarningsExact identifier
spl id: 24b27c05-e17d-083d-e063-6394a90a0fe7
spl set id: ba5cd48c-cd43-2f63-e053-2a95a90a930f

Reported adverse events (FAERS/openFDA)#

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