Lidothal Relief

Manufacturer
Henan Kangdi Medical Devices Co. Ltd.
Effective date
2017-07-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:06

Label at a glance#

ProductLidothal Relief
Active ingredientMENTHOL, LIDOCAINE
Label structure9 sections

Storage and handling

Store at room temperature. Avoid direct sunlight.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol  1.00%

Lidocaine 4.00%

OTC - PURPOSE SECTION

Purpose

External analgesic

External analgesic

INDICATIONS & USAGE SECTION

Uses:

For temporary relief of minor aches and pains of the muscles and joints associated with simple backache, arthritis, strains,

bruises and sprains

WARNINGS SECTION

Warnings:

  • For external use only
  • Avoid contact with eyes
  • Do not apply to open wounds or damages skin
  • If symptoms persist for more than seven days, discontinue use and consult physician
  • Keep out of reach of children. If swallowed, consult physician.
  • Do not bandage tightly
  • If pregnant or breast feeding, contact physician prior to use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, consult physician.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Clean and dry affected area
  • Remove patch from backing and apply to affected area. Apply directly to affected area.
  • Use only on patch at a time, and a maximum of four patches per day.
  • Leave patch of affected area for up to eight hours.
  • Do not use patches for more than five consecutive days
  • Children under 12 should consult a physician prior to use.

STORAGE AND HANDLING SECTION

Store at room temperature. Avoid direct sunlight.

INACTIVE INGREDIENT SECTION

Other Ingredients:

acrylic acid ,aluminum hydroxide . carmellose sodium 2-ethylexyl acrylate glycerin . isopropyl myristate .methyl acrylate

nonoxynol-30 .poluacrylate.polyacrylic acid .polysorbate 80 sorbitan sesquioleate strach .talc .tartaric acid

.titanium dioxide .water(254-114)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1249758lidocaine 4 % / menthol 1 % Medicated PatchPSN1
1249758lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD1
1249758lidocaine 4 % / menthol 1 % 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
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69561-463-152020-01-31C16284748780-19d75b9d0-e37a-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69561-463-15Lidothal Relief8.5 g in 1 PATCHPATCH8.51
69561-463-15Lidothal Relief15 in 1 BOXPATCH151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69561-463LIDOTHAL RELIEF (MENTHOL, LIDOCAINE) PATCH [HENAN KANGDI MEDICAL DEVICES CO. LTD.]1Legacy NDC, 2 package rows20170801_ea887561-16b0-4b5d-b544-5b74e6b413ba.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69561-46369561-463-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
89072c07-9695-4c5e-83fc-81eaa488b929ea887561-16b0-4b5d-b544-5b74e6b413ba2017-07-31WarningsExact identifier
spl id: 89072c07-9695-4c5e-83fc-81eaa488b929
spl set id: ea887561-16b0-4b5d-b544-5b74e6b413ba

Reported adverse events (FAERS/openFDA)#

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