LidoFore 4% FlexiPatch

Manufacturer
Greenhill Trading, Inc.
Effective date
2022-06-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:59:12

Label at a glance#

ProductLidoFore 4% FlexiPatch
Active ingredientLIDOCAINE
Label structure13 sections

Indications and uses

For the temporary relief of pain

Storage and handling

Avoid storing product in direct sunlight Protect product from excessive moisture

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Uses:

INDICATIONS & USAGE SECTION

For the temporary relief of pain

WARNINGS:

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use

  • more than 1 pathch at a time
  • on wounds or damaged skin
  • with a heating pad
  • if you are allergic to any ingredients of this product

OTC - WHEN USING SECTION

When using this product

  • use only as directed
  • avoid contact with the eyes, mucous membranes or rashes
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask a doctor if

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If Pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 12 years of age and over:

  • Clean and dry the affected area
  • Open pouch and remove one patch
  • Apply 1 patch at a time to affected area; not more than 3 to 4 times daily
  • Reseal pouch containing unused patches after each use
  • 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
  • Protect product from excessive moisture

INACTIVE INGREDIENT SECTION

Other ingredients: Acrylic Adhesive, Flaxseed oil, and Polysorbate 80

Questions or comments? 347-378-2800

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaged For: Greenhill Trading Inc.
Brookly, NY 11233
Questions and Information.
Phone: 347-378-2800

PRINCIPAL DISPLAY PANEL - 40 mg LabelPRINCIPAL DISPLAY PANEL - 40 mg Label

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
82219-310-10EA - Each82219-3108fd87fe3-e7bd-47f5-ba21-f79fedeabdfe12022-07-06

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82219-31082219-310-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
2b54fe19-c27e-48c5-bf80-a971c93ee17e14246ae9-25cb-4f61-8185-3f0cdaf4ea9a2022-09-28WarningsExact identifier
spl set id: 14246ae9-25cb-4f61-8185-3f0cdaf4ea9a

Reported adverse events (FAERS/openFDA)#

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