79740-009 更新信息 TIDL PAIN RELIEF NUMBING PATCH

Manufacturer
The Anthos Group
Effective date
2024-02-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:08:53

Label at a glance#

ProductTIDL PAIN RELIEF NUMBING TIDL
Active ingredientMENTHOL, LIDOCAINE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%,

Menthol 3%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses Temporary relief from minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and sprains

WARNINGS SECTION

Wamings
For extemal use only .
Do not use a on puncture wounds , cuts , imitated , damaged or swollen skin
more than 1 path 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 his product
use only as directed
do not bandage tighty
avoid contact with eyes and mucous membranes
rare cases of serous bums have been reported with products of this type
a transient buming sensation may occur upon application but enerally disappears in several days
dispose of used patch in manner hat always keeps products away from children and pets . Used patches still contain e g po at can po s ad fs f a hid or pt chews or ingests this patch
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days
symptoms ear up and occur again within a few days
severe burning sensation, redness or irritation develops
you experience signs of skin inur , such as pain , sw , or blistering where the product was appliedIf pregnant or breast-feeing , ask a health professional efore use . ep out of each of hilden .If swallowed , get medical help or contact a Poison Control Center night away

INACTIVE INGREDIENT SECTION

Purity Water, 059QF0KO0R
Glycerol, PDC6A3C0OX
Sodium polyacrylate, 05I15JNI2J
Wintergreen Oil, LAV5U5022Y
Ethanol, 3K9958V90M
Tartaric acid, W4888I119H
Aluminum Glycinate, 1K713C615K
Chilli extract, 00UK7646FG
EDTA-2NA, 9G34HU7RV0

DOSAGE & ADMINISTRATION SECTION

one slice at a time

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79740-009-1 5 BAG in 1 BOX

79740-009-1 5 BAG in 1 BOX79740-009-1 5 BAG in 1 BOX

79740-009-2 1 PATCH in 1 BAG

79740-009-2 1 PATCH in 1 BAG79740-009-2 1 PATCH in 1 BAG

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1649008lidocaine 4 % / menthol 3 % Medicated PatchPSN2
1649008lidocaine 0.04 MG/MG / menthol 0.03 MG/MG Medicated PatchSCD2
1649008lidocaine 4 % / menthol 3 % Medicated PatchSY2

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79740-009-01TIDL PAIN RELIEF NUMBINGTIDL5 in 1 BOXPATCH52
79740-009-02TIDL PAIN RELIEF NUMBINGTIDL1 in 1 BAGPATCH12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79740-009TIDL PAIN RELIEF NUMBING TIDL (PAIN RELIEF) PATCH [THE ANTHOS GROUP]2Legacy NDC, 2 package rows20240223_e815287d-d589-2854-e053-2a95a90ad940.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
79740-00979740-009-02, 79740-009-01

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
11e6d987-e028-8685-e063-6394a90a239be815287d-d589-2854-e053-2a95a90ad9402024-02-21WarningsExact identifier
spl id: 11e6d987-e028-8685-e063-6394a90a239b
spl set id: e815287d-d589-2854-e053-2a95a90ad940

Reported adverse events (FAERS/openFDA)#

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