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OTC products · Product label record

Relieved Pro Wrap drug information

4% LIDOCAINE PATCH
Transfer Technology · TOPICAL

Product NDC: 71662-004

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic name4% LIDOCAINE PATCH
Labeler / manufacturerTransfer Technology
RouteTOPICAL
Drug classAmide Local Anesthetic / Antiarrhythmic
Product NDC71662-004
Label effective date2026-08-28

Official product label reference

Relieved Pro Wrap — Transfer Technology

This page contains 13 source sections for 4% LIDOCAINE PATCH, topical route. Label set 5a1c6ebf-ad3f-c47b-e063-6294a90aa19a, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose

Use Use For the temporary relief of pain.
Dosage and administration — label text
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
Warnings
Warnings 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
Active ingredient
Active Ingredient Active Ingredient: 4% Lidocaine
Do not use
Do Not Use Do not use If you are allergic to Lidocaine. On open wounds or damaged,, broken or iritated skin.
Ask a doctor before use
Ask your doctor 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.
While using this medicine
When using this product 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
When to stop use and seek help
Stop use if Conditions worsens Symptoms persist for more than 7 days
Pregnancy
If pregnant or breast feeding If pregnant or breast feeding ask a physician before use.
Child safety
Keep out of reach of children 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
Storage and handling
Other information store at room termperature Do not exceed 100 o Fahrenheit, 38 o Celsius
Inactive ingredient
Inactive ingredients Inactive ingredients Acrylic Adhesive Cotton fabric

Official sources and product identifiers

Substances listed: LIDOCAINE

RxNorm identifiers: 1737778

Package NDC codes

71662-004-10

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.