Relieved Pro Wrap

Manufacturer
Transfer Technology
Effective date
2026-08-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-01 13:03:19

Label at a glance#

ProductRelieved Pro Wrap
Active ingredientLIDOCAINE
Label structure14 sections

Indications and uses

For the temporary relief of pain Peel patch off plastic liner and place lpatch on affected area for no more than 12 hours

Storage and handling

store at room termperature Do not exceed 100 o Fahrenheit, 38 o Celsius

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: 4% Lidocaine

Use

OTC - PURPOSE SECTION

Use

For the temporary relief of pain.

Indications and usage

INDICATIONS & USAGE SECTION

  • For the temporary relief of pain
  • Peel patch off plastic liner and place lpatch on affected area for no more than 12 hours

Warnings

WARNINGS SECTION

For external use only The adhesion 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

Do not use

If you are allergic to Lidocaine. On open wounds or damaged,, broken or iritated skin.

Ask your doctor

OTC - ASK DOCTOR SECTION

Ask your doctor or pharmacist before use if you are using blood thinning medication, steroids, or non-sterodial and anti-inflammatory drugs (NSAIDs), or if you have sensitive skin.

When using this product

OTC - WHEN USING SECTION

When using this product

  • 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

Stop use if

OTC - STOP USE SECTION

  • Conditions worsens
  • Symptoms persist for more than 7 days

If pregnant or breast feeding

PREGNANCY SECTION

If pregnant or breast feeding ask a physician before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • store at room termperature
  • Do not exceed 100 o Fahrenheit, 38 o Celsius

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients

Acrylic Adhesive

Cotton fabric

Dosage & Administration Section

Directions adults/children 12 years or older

  • 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 physcian before use.
  • For easier removal of the patch, apply rubbing alcohol or baby oil to adhesvie edge while gently peeling

Relieved Pro Wrap

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Relieved Pro Wrap

Pro WrapPro Wrap

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
71662-00471662-004-10

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
Relieved Pro Wrap4% LIDOCAINE PATCHTransfer Technology5a1c6ebf-ad3f-c47b-e063-6294a90aa19a2026-08-28WarningsExact identifier
ndc (package): 71662-004-10
ndc (product): 71662-004
ndc11 (package): 71662000410
spl id: 5a1c6ebf-ad40-c47b-e063-6294a90aa19a
spl set id: 5a1c6ebf-ad3f-c47b-e063-6294a90aa19a

Reported adverse events (FAERS/openFDA)#

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