MediRelief Lidocaine 4% Patch

Manufacturer: FARLA MEDICAL HEALTHCARE LTD
Effective date: 2024-02-23
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 21:10:53

Label at a glance#

ProductMediRelief

Active ingredientLIDOCAINE

Label structure7 sections

Indications and uses

For the temporary relief of pain.

Dosage and administration

adults & children 12 years of age and older: apply to affected area not more than 3 to 4 times daily - clean dry affected area - remove film from patch and apply to skin (see illustration) children under 12 years of age: consult a doctor

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Active Ingredients & Purpose

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredients (in each patch) Purpose

Lidocaine 4%..............................................................................................Topical analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY. Avoid contact with the eyes.

Do not use

OTC - DO NOT USE SECTION

in large quantities, particularly over raw surfaces or blistered areas
on sensitive skin
if allergic to any ingredients in this product

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens
redness is present
symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant of breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

adults & children 12 years of age and older: apply to affected area not more than 3 to 4 times daily

- clean dry affected area

- remove film from patch and apply to skin (see illustration)

children under 12 years of age: consult a doctor

Other Information

OTHER SAFETY INFORMATION

store at room temperature 68-77°F (20-25°C)
do not store in direct sunlight or expose to excessive heat and moisture

TAMPER EVIDENT: Do not use if pouch containing the patch is torn or broken.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

dihydroxyaluminum aminoacetate, glycerin, kaolin, methylparaben, polyacrylic acid, polysorbate 80, povidones, propylene glycol, propylparaben, sodium polyacrylate, tartaric acid, titanium dioxide, water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 73486-102-25
Count: (3.9”x5.5”) 5 Patches Box

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73486-102-25	2024-02-26	C162847	48780-1	1030e365-2c11-111a-e063-dadaa90a10e2	MediRelief Lidocaine 4% Patch
73486-102-25	2024-01-30	C162847	48780-1	1030e365-2c11-111a-e063-dadaa90a10e2	MediRelief Lidocaine 4% Patch

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73486-102	MEDIRELIEF (LIDOCAINE) PATCH [FARLA MEDICAL HEALTHCARE LTD]	5	Legacy NDC	20240228_a698cdbc-6e34-164d-e053-2a95a90ab4d2.zip

Products#

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

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

MediRelief
Lidocaine
PROPYLPARABEN
PROPYLENE GLYCOL
WATER
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS
POVIDONE
METHYLPARABEN
KAOLIN
POLYSORBATE 80
POLYACRYLIC ACID (250000 MW)
TITANIUM DIOXIDE
TARTARIC ACID
GLYCERIN
SODIUM POLYACRYLATE (8000 MW)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73486-102	73486-102-25

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
PROPYLPARABEN	Z8IX2SC1OH	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS	1K713C615K	IACT
POVIDONE	FZ989GH94E	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
KAOLIN	24H4NWX5CO	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
POLYACRYLIC ACID (250000 MW)	9G2MAD7J6W	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
TARTARIC ACID	W4888I119H	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM POLYACRYLATE (8000 MW)	285CYO341L	IACT
LIDOCAINE	98PI200987	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
46a1f276-c61e-3299-e063-6294a90ab962			a698cdbc-6e34-164d-e053-2a95a90ab4d2	2025-12-23	Warnings	Exact identifier spl set id: a698cdbc-6e34-164d-e053-2a95a90ab4d2

Reported adverse events (FAERS/openFDA)#

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