LK Herbal Patch

Manufacturer
CAI Industries Corp.
Effective date
2025-08-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:11:24

Label at a glance#

ProductLK Herbal Patch
Active ingredientLEVOMENTHOL
Label structure8 sections

Indications and uses

Temporarily relieves muscle and joint pains: backaches, arthritis, strains, bruises, sprains

Dosage and administration

Adults and children 12 years of age and older : cut plaster to ideal size, remove clear film and apply to affected area Avoid over 8 hours of continuous usage or consult your physician Do not apply on extermely hairy skin Wet the patch with warm water before removing Children under 12 years of age : consult your physician

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 5.1%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves muscle and joint pains: backaches, arthritis, strains, bruises, sprains

Warnings

WARNINGS SECTION

For external use only

When using this product 

  • avoid contact with the eyes or mucous membranes 
  • do not use on wounds or broken skin

Stop use and ask a doctor if

  • conditions worsen 
  • excessive skin irritation develops
  • nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash occurs
  • symptoms persists for more than 7 days

If pregnant or breast-feeding, ask a doctor before use.

Keep out of reach of children. 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: cut plaster to ideal size, remove clear film and apply to affected area
  • Avoid over 8 hours of continuous usage or consult your physician
  • Do not apply on extermely hairy skin
  • Wet the patch with warm water before removing
  • Children under 12 years of age: consult your physician

Other Information

SPL UNCLASSIFIED SECTION

  • Keep unused plasters in the pouch
  • Store in a cool dry place at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Chuan Wu ACONITUM CARMICHAELII ROOT, Cao Wu (ACONITUM KUSNEZOFFII LEAF), Di Huang - Radix Rehmanniae, Bai Lian AMPELOPSIS JAPONICA TUBER, Bai Zhi - ANGELICA DAHURICA ROOT, Dang Gui (ANGELICA SINENSIS ROOT), Chi Shao whole PAEONIA LACTIFLORA WHOLE, Qiang Huo whole (HANSENIA FORBESII WHOLE, Wu Yao - LINDERA AGGREGATA ROOT, Gan Cao (LICORICE), Du Huo (ANGELICA PUBESCENS ROOT), Xuan Shen (SCROPHULARIA NINGPOENSIS ROOT), Da Huang ( RHEUM OFFICINALE ROOT), Liu Zhi (SOLIDAGO VIRGAUREA FLOWERING TOP, Methyl salicylate

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2722188menthol 5.1 % Medicated PatchPSN1
2722188menthol 0.051 MG/MG Medicated PatchSCD1
2722188menthol 5.1 % Medicated PatchSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85954-002-01LK Herbal Patch10 in 1 PACKAGEPATCH101

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85954-00285954-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
575eece4-286c-0fcc-e063-6294a90a7bcfc56241b3-ef7a-40ee-a89a-754a580b01182026-07-24WarningsExact identifier
spl set id: c56241b3-ef7a-40ee-a89a-754a580b0118

Reported adverse events (FAERS/openFDA)#

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