Well Lido Gel Patch

Manufacturer
True Marker Pharmaceuticals, Inc.
Effective date
2024-09-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:54:56

Label at a glance#

ProductWell Lido Gel Patch
Active ingredientLIDOCAINE
Label structure7 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 that 3 to 4 times a daily • Remove patch from the skin after at most 8-hour application • Children under 12 year of age. Consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients                         Purposes

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%                                Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of pain.

Warnings

WARNINGS SECTION

For External Use only.

Stop use and ask a doctor

  • Localized skin reaction occur, such as rash, itching, redness, irritation, pain, swelling and blistering
  • Condition worsens
  • Symptoms persist for more than 7 days
  • Symptoms clear up and occur again within a few days

Keep out of the reach of children
If swallowed, get medical help or contact Poison Control Center right away.

Do Not Use
• More than 1 patch a time
• On wounds or damaged skin
• With a heating pad
• If you are allergic to any ingredients of this product

If pregnant or Breast-Feeding
Ask a health professional before use

When Using this product
• Use only as directed
• Avoid contact with eyes, mucous membranes or rashes
• Do not bandage tightly

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 that 3 to 4 times a daily
• Remove patch from the skin after at most 8-hour application
• Children under 12 year of age. Consult a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Dihydroxyaluminum aminoacetate, Edetate disodium, Glycerin, Kaolin, Methylparaben, Polyacrylic acid, Polysorbate 80, Polyvinylpyrrolidone K90, Propylene glycol, propylparaben, sodium polyacrylate, tartaric acid, titanium dioxide, water.

Other Information

SPL UNCLASSIFIED SECTION

• Store at controlled room temperature 68º-77ºF (20º-25ºC)
• Avoid storing product in direct sunlight
• Protect product from excessive moisture

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83592-07183592-071-15

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

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
27eb8820-db9f-725e-e063-6394a90adf49d03aa7d0-7ed1-4a41-9763-38dbc642b9bd2024-11-27WarningsExact identifier
spl set id: d03aa7d0-7ed1-4a41-9763-38dbc642b9bd

Reported adverse events (FAERS/openFDA)#

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