YYBA - Welmate Lidocaine Pain Relieving Patch (73581-001)

Manufacturer
YYBA CORP
Effective date
2026-09-07
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-09-10 00:00:56

Label at a glance#

ProductPain Relieving Lidocaine Patch
Active ingredientLIDOCAINE
Label structure12 sections

Indications and uses

Temporarily relieves minor pain

Dosage and administration

Adults and children over 12 years: clean and dry affected area remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle carefully remove from the skin after at most 8-hour application apply to the affected area not more than 3 to 4 times daily children 12 years or younger: ask a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

  • more than 1 patch on your body at a time or on cut, irritated or swollen skin
  • on puncture wounds or damaged skin
  • with a heating pad
  • if you are allergic to ingredients of this product

When Using This Product

OTC - WHEN USING SECTION

  • use only as directed. Read and follow all directions and warnings on this label.
  • do not allow contact with the eyes
  • do not bandage tightly or apply local heat (such as heating pads) to the area of use
  • do not use at the same time as other topical analgesics
  • dispose of used patch in manner that always keeps product away from children or pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

Stop Use and Ask a Doctor if

OTC - STOP USE SECTION

  • condition worsens
  • redness is present
  • irritation develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied
  • symptoms clear up and occur again within few days

If Pregnant or Breast Feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep Out of Reach of Children and Pets

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

Adults and children over 12 years:

  • clean and dry affected area
  • remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle
  • carefully remove from the skin after at most 8-hour application
  • apply to the affected area not more than 3 to 4 times daily

children 12 years or younger:ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

dihydroxyaluminium aminoacetate, disodium EDTA, glycerin, methylparaben, polyvinyl alcohol, propyl paraben, propylene glycol, purified water, sodium carboxymethyl cellulose, sodium polyacrylate, tartaric acid, titanium oxide

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1V1V

4040

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73581-00173581-001-30, 73581-001-40, 73581-001-03, 73581-001-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62026-01-14full-release2026-06-01 01:33:20
52025-11-14monthly-update2026-06-03 17:40:07

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
Pain Relieving Lidocaine PatchLIDOCAINEYYBA CORPaf8c84fd-224c-72b3-e053-2a95a90a95682026-09-07WarningsExact identifier
ndc (package): 73581-001-40
ndc (package): 73581-001-30
ndc (package): 73581-001-10
ndc (package): 73581-001-03
ndc (product): 73581-001
ndc11 (package): 73581000140
ndc11 (package): 73581000130
ndc11 (package): 73581000110
ndc11 (package): 73581000103
spl id: 5ae664f1-d4da-d372-e063-6394a90a5ea3
spl set id: af8c84fd-224c-72b3-e053-2a95a90a9568

Reported adverse events (FAERS/openFDA)#

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