Relevea Pain Relief Patch

Manufacturer
Links Medical Products
Effective date
2026-09-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-09-26 01:01:02

Label at a glance#

ProductRelevea Pain Relief Patch
Active ingredientLIDOCAINE
Label structure9 sections

Indications and uses

for temporary relief of pain

Dosage and administration

Adult and children 12 years of age and over: clean and dry affected area remove film from patch and apply to the skin apply 1 patch at a time to affected area, not more than 3 to 4 times daily remove patch from the skin after at most 8-hour application Children under 12 years of age: Consult a doctor

Storage and handling

avoid storing product in direct sunlight and protect product from excessive moisture.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

PURPOSE

OTC - PURPOSE SECTION

Topical anesthetic

USES

INDICATIONS & USAGE SECTION

for temporary relief of pain

WARNINGS

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • more than 1 patch at a time
  • 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
  • do not bandage

Stop use and ask a doctor if

OTC - STOP USE SECTION

localized skin reactions such as rash, itching, redness, irritation, pain, swelling and blistering occur, conditions worsen, symptoms persist for more than 7 days, or symptoms clear up and occur again within a few days.

If pregnant or breast feeding, 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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adult and children 12 years of age and over:

  • clean and dry affected area
  • remove film from patch and apply to the skin
  • apply 1 patch at a time to affected area, not more than 3 to 4 times daily
  • remove patch from the skin after at most 8-hour application

Children under 12 years of age: Consult a doctor

OTHER INFORMATION

STORAGE AND HANDLING SECTION

avoid storing product in direct sunlight and protect product from excessive moisture.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Methylparaben, Polysorbate 80, Propylene Glycol, Polyacrylic Acid, Polyvinylpyrrolidone K90, Propylparaben, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Water

Questions or Comments

OTC - QUESTIONS SECTION

888.425.1149

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PouchPouchBoxBox

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130351028004038GTIN-13: 0351028004038
EAN-13: 0351028004038
GTIN-12: 351028004038
UPC-A: 351028004038
GTIN storage (14 digits): 00351028004038
Relevea pouch_1 count_9.23.26.jpg
BarcodeEAN-130351028004151GTIN-13: 0351028004151
EAN-13: 0351028004151
GTIN-12: 351028004151
UPC-A: 351028004151
GTIN storage (14 digits): 00351028004151
Relevea box_15 count_9.23.26.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51028-00451028-004-01, 51028-004-02, 51028-004-03, 51028-004-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-09-10daily-update2026-09-12 01:01:26
22026-08-23daily-update2026-08-26 01:01:18
12025-08-21full-release2026-06-01 01:38:48

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
5b210dcd-a455-d8f3-e063-6294a90af8b43ce49b85-e9e3-e33c-e063-6294a90a6dbf2026-09-10WarningsExact identifier
spl set id: 3ce49b85-e9e3-e33c-e063-6294a90a6dbf

Reported adverse events (FAERS/openFDA)#

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