MEIJER PAIN RELIEF PATCHES

Manufacturer
Meijer Distribution Inc | Foshan Aqua Gel Biotech Co.,Ltd.
Effective date
2024-12-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:44:51

Label at a glance#

ProductMEIJER PAIN RELIEF PATCHES
Active ingredientLIDOCAINE
Label structure14 sections

Dosage and administration

Directions 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 smaller portion of backing from patch and apply exposed portion of patch to affected area ■ once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected ar...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4% . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Topical Anesthetic

Purpose

OTC - PURPOSE SECTION

Temporarily relieves minor pain.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Directions 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 smaller portion of backing from patch and apply exposed portion of patch to affected area

■ once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area

■ use one patch for up to 12 hours. Children under 12 years of age: consult a physician.

Warnings

WARNINGS SECTION

For external use only.

Idications and Usage

INDICATIONS & USAGE SECTION

Uses: Temporaily relieves minor pains.

When using this product

OTC - WHEN USING SECTION

■ use only as directed

■ read and follow all directions and warnings on this carton

■ do not allow contact with the eyes

■ do not use at the same time as other topical analgesics

■ 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 consult a doctor

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

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.

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.

Other Safety Information

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aluminum Glycinate, Glycerin, Kaolin, Methylparaben, Polyacrylic Acid, Polysorbate 80, Propylene Glycol,
Propylparaben, PVP, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Water

Questions

OTC - QUESTIONS SECTION

TOLL-FREE

Customer Care Help Line
866-326-1313
Mon–Fri 8:30 am–4:30 pm CST

DIST. BY
MEIJER DISTRIBUTION, INC.
GRAND RAPIDS, MI 49544
www.meijer.com


Made in China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lidocaine Patch
Lidocaine Patch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737778lidocaine 4 % Medicated PatchPSN4
1737778lidocaine 0.04 MG/MG Medicated PatchSCD4
1737778lidocaine 4 % Medicated PatchSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41250-972-052021-12-17C16284748780-19d75b9d0-e374-f424-e053-dadaa90a57ceMEIJER PAIN RELIEF PATCHES
41250-972-052020-01-31C16284748780-19d75b9d0-e374-f424-e053-dadaa90a57ceMEIJER PAIN RELIEF PATCHES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-972-05MEIJER PAIN RELIEF PATCHES5 in 1 CARTONPATCH54
41250-972-05MEIJER PAIN RELIEF PATCHES9 g in 1 PATCHPATCH94

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-972MEIJER PAIN RELIEF PATCHES (LIDOCAINE) PATCH [MEIJER DISTRIBUTION INC]4Current NDC, Legacy NDC, 2 package rows20241220_aa5da66d-3ba9-4120-be35-44bec475761a.zip

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
41250-97241250-972-05

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 · Source PDF

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
MEIJER PAIN RELIEF PATCHESLIDOCAINEMeijer Distribution Incaa5da66d-3ba9-4120-be35-44bec475761a2024-12-18WarningsExact identifier
ndc (package): 41250-972-05
ndc (product): 41250-972
ndc11 (package): 41250097205
spl id: 29925cee-2e07-e2a7-e063-6394a90ac830
spl set id: aa5da66d-3ba9-4120-be35-44bec475761a

Reported adverse events (FAERS/openFDA)#

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