Tidl Pain Relief Numbing Patch

Manufacturer
Fuzhou Ayimong Trading Co., Ltd.
Effective date
2024-03-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:10:14

Label at a glance#

ProductTidl Pain Relief Numbing Patch
Active ingredientMENTHOL, LIDOCAINE
Label structure12 sections

Dosage and administration

Adults and children 12 years of age and older: -clean and dry affected area -remove backing from patch by firmly grasping both ends and gently pulling until backing seprarates in middle -carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area -once exposed portion of the patch is positioned,carefully remove remaining backing to completely apply patch to affected a...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%
Menthol 3%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Use

INDICATIONS & USAGE SECTION

for the temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

·on puncture wounds,cuts,irritated,damaged or swollwn skin

·more than 1 patch on your body at a time or with other topical analgesics at the same time

·with a heating pad or apply local heat to the area of use

When Using

OTC - WHEN USING SECTION

·use only as directed

·do not bandage tightly

·avoid contact with eyes and mucous membranes

·rare cases of serious burns have been reported with products of this type

·a transient burning sensation may occur upon application but generally disappears in several days

·dispose of used patch in manner that always keeps products 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

OTC - STOP USE SECTION

·condition worsens or symptoms persist for more than 7 days
·symptoms clear up and occur again within a few days
·severe burning sensation,redness or irritation develops
·you experience signs of skin injury,such as pain,swelling,or blistering where the product was applied

Ask Doctor

OTC - ASK DOCTOR SECTION

·condition worsens or symptoms persist for more than 7 days
·symptoms clear up and occur again within a few days
·severe burning sensation,redness or irritation develops
·you experience signs of skin injury,such as pain,swelling,or blistering where the product was applied

Keep Oot 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 of age and older:
-clean and dry affected area
-remove backing from patch by firmly grasping both ends and gently pulling until backing seprarates in middle
-carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area
-once exposed portion of the patch is positioned,carefully remove remaining backing to completely apply patch
to affected area - use 1 patch at a time and not more than 3 to 4 times daily
Children under 12 years of age: consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aluminum glycinate, chili extract, EDTA-2NA, ethanol, glycerol, sodium polyacrylate, tartaric acid,
water, wintergreen oil

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1649008lidocaine 4 % / menthol 3 % Medicated PatchPSN1
1649008lidocaine 0.04 MG/MG / menthol 0.03 MG/MG Medicated PatchSCD1
1649008lidocaine 4 % / menthol 3 % Medicated PatchSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83822-003-012025-07-29C16284748780-13b156c62-2643-fb37-e063-e6dba90a4e0783822-003

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83822-003-01Tidl Pain Relief Numbing Patch20 in 1 BOXPATCH201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83822-003TIDL PAIN RELIEF NUMBING PATCH (PAIN RELIEF PATCH) PATCH [FUZHOU AYIMONG TRADING CO., LTD.]11 package rows20240325_145f7499-b92c-f953-e063-6294a90a36e4.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83822-00383822-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
145f7499-b92d-f953-e063-6294a90a36e4145f7499-b92c-f953-e063-6294a90a36e42024-03-23WarningsExact identifier
spl id: 145f7499-b92d-f953-e063-6294a90a36e4
spl set id: 145f7499-b92c-f953-e063-6294a90a36e4

Reported adverse events (FAERS/openFDA)#

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