Re-Lieved Lidocaine Patch

Manufacturer
Transfer Technology | Transfer Technoloy
Effective date
2024-12-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:49:28

Label at a glance#

ProductRe-Lieved Lidocaine Patch
Active ingredientLIDOCAINE
Label structure14 sections

Indications and uses

For the temporary relief of pain.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

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.

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 o Fahrenheit, 38 o Celsius

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylic adhesive, Polyethylene/Natural fiber fabric blend

Re-Lieved Lidocaine 4% 20 Cloth Patches in Indivdual Pouches

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Relieved Lidocaine 4% 20 CountRelieved Lidocaine 4% 20 Count

Drug Facts PanelDrug Facts Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737778lidocaine 4 % Medicated PatchPSN3
1737778lidocaine 0.04 MG/MG Medicated PatchSCD3
1737778lidocaine 4 % Medicated PatchSY3

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
71662-010-20Re-Lieved Lidocaine Patch4 mg in 1 POUCHPATCH43

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71662-010RE-LIEVED LIDOCAINE PATCH (LIDOCAINE PATCH 4%) PATCH [TRANSFER TECHNOLOGY]31 package rows20241229_f6c9c88c-37d6-5bbb-e053-6294a90af466.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71662-010-20EA - Each71662-0103a6fc109-e0b5-4e4e-8217-575a1c51b4f512023-04-07

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71662-01071662-010-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 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
2a57fbd9-78ca-9dd3-e063-6394a90acc63f6c9c88c-37d6-5bbb-e053-6294a90af4662024-12-28WarningsExact identifier
spl id: 2a57fbd9-78ca-9dd3-e063-6394a90acc63
spl set id: f6c9c88c-37d6-5bbb-e053-6294a90af466

Reported adverse events (FAERS/openFDA)#

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