Walgreens Lidocaine 4% Patch Back, 6 patches

Manufacturer: Walgreen Co. | Planet (Anhui) Pharmaceutical Co. Ltd
Effective date: 2025-04-25
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:59:48

Label at a glance#

ProductWalgreens Lidocaine Back

Active ingredientLIDOCAINE

Label structure7 sections

Dosage and administration

Adults and children 12 years if age and over: Clean and dry affected area Carefully remove backing from patch Apply sticky side of patch to affected area Use one patch for up to 8 hours Discard patch after single use Apply 1 patch at a time to affected area, not more than 3 to 4 times daily Children under 12 years of age: consult a physician.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

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 one patch on your body at a time
On cut, irritated or swollen skin
On puncture wounds
For more than one week without consulting a doctor
If you are allergic to any active or inactive ingredients
If pouch is damaged or opened

When using this product

OTC - WHEN USING SECTION

Use only as directed
Read and follow all directions and warnings
Do not allow contact with the eyes
Do not use at the same time as other topical anesthetics
Do not bandage tightly or apply local heat (such as heating pads) to the area of use
Do not microwave
Dispose of used patch in manner that always keeps product away from children and 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 worsen
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

If pregnant or 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 and children 12 years if age and over:

Clean and dry affected area
Carefully remove backing from patch
Apply sticky side of patch to affected area
Use one patch for up to 8 hours
Discard patch after single use
Apply 1 patch at a time to affected area, not more than 3 to 4 times daily

Children under 12 years of age:consult a physician.

Other information

SPL UNCLASSIFIED SECTION

Store in a clean, dry place outside of direct sunlight
Protect from excessive moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

A-tocopherol Acetate, CMC-2Na, Dihydroxyaluminum Aminoacetate, Fumed Silica, Glycerol, Laurocapram, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Polyacrylic Acid, Propylene Glycol, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Urea, Vanillyl Butyl Ether, Water, 3-2-(Ethylhexyl)oxyl-1, 2-Propanediol.

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1737778	lidocaine 4 % Medicated Patch	PSN	2
1737778	lidocaine 0.04 MG/MG Medicated Patch	SCD	2
1737778	lidocaine 4 % Medicated Patch	SY	2

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
LIDOCAINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-2178-01	Walgreens Lidocaine Back	1 in 1 BAG	PATCH	1		2
0363-2178-01	Walgreens Lidocaine Back	6 in 1 BOX	PATCH	6		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-2178	WALGREENS LIDOCAINE BACK (LIDOCAINE) PATCH [WALGREEN CO.]	2	Current NDC, 2 package rows	20250427_e6bfd342-c0db-46b9-b5e6-5acbd860adf1.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

Walgreens Lidocaine Back
LIDOCAINE
.ALPHA.-TOCOPHEROL ACETATE
DIHYDROXYALUMINUM AMINOACETATE
GLYCERIN
LAUROCAPRAM
PEG-40 HYDROGENATED CASTOR OIL
PHENOXYETHANOL
PROPYLENE GLYCOL
TARTARIC ACID
TITANIUM DIOXIDE
UREA
VANILLYL BUTYL ETHER
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0363-2178	0363-2178-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
DIHYDROXYALUMINUM AMINOACETATE	DO250MG0W6	IACT
GLYCERIN	PDC6A3C0OX	IACT
LAUROCAPRAM	1F3X9DRV9X	IACT
PEG-40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
TARTARIC ACID	W4888I119H	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
UREA	8W8T17847W	IACT
VANILLYL BUTYL ETHER	S2ULN37C9R	IACT
WATER	059QF0KO0R	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
Walgreens Lidocaine Back	LIDOCAINE	Walgreen Co.	e6bfd342-c0db-46b9-b5e6-5acbd860adf1	2025-04-25	Warnings	Exact identifier ndc (package): 0363-2178-01 ndc (product): 0363-2178 ndc11 (package): 00363217801 spl id: 33998f45-f222-883d-e063-6294a90ad003 spl set id: e6bfd342-c0db-46b9-b5e6-5acbd860adf1

Reported adverse events (FAERS/openFDA)#

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