Lekon Herbal Patch Green

Manufacturer
Taiwan Three Mast Pharmaceutical Company Limited
Effective date
2014-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:20

Label at a glance#

ProductLekon Herbal Patch Green
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure9 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints due to: backache, arthritis, strains, bruises, sprains.

Dosage and administration

• Remove clear film and apply to sore area of skin.    Use no more than 3times daily. • Bandage will remain effective after 24 hours and will be even more effective if used after a bath. Do not apply on extremely hairy skin. Highly      adhesive plaster may hurt skin upon removal. • For children under 12 years of age, consult a doctor before use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Menthol 5.1%
Camphor 3%

PURPOSE

OTC - PURPOSE SECTION

External analgesic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

USES:

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints due to: backache, arthritis, strains, bruises, sprains.

WARNINGS SECTION

WARNING: 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:
• condition worsens
• excessive skin irritation develops
• nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs
• symptoms persist for more than 7 days
If pregnant or breast-feeding, ask a doctor before use.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

• Remove clear film and apply to sore area of skin.
   Use no more than 3times daily.
• Bandage will remain effective after 24 hours and will be even more effective if used after a bath. Do not apply on extremely hairy skin. Highly      adhesive plaster may hurt skin upon removal.
• For children under 12 years of age, consult a doctor before use.

OTHER INGREDIENTS:

INACTIVE INGREDIENT SECTION

Chuan Wu (Radix Aconiti Preparata), Cao Wu (Radix Aconiti Kusnezoffii Preparata), Di Huang (Radix Rehmanniae), Bai Lain (Radix Ampelopsis Japonicae), Bai ji(Rhizome Bletilla), Gui Zhi(Radix Angelicae Sinesis), Bai zhi(Radix Angelicae Dahuricae), Dang Gui(Radix Angelicae Sinesis), Chi Shao (Radix Rubrus Paeoniae Lactiflorae), Qiang Huo (Radix Et Rhizoma Notopterygii), Ku Shen(Radix Sophorae Flavescentis), Wu yao (Radix Linderae Strychnifoliae), Gan Cao (Radix Glycyrrhizae), Du Huo (Radix Angelicae Pubescentis), Xuan Shen(Radix Scrophulariae Ningpoensis), Da Huang (Radix Et Rhizoma Rhei), Liu Zhi (Ramulus Salicis Babylonicae), Dong Qing Oil (LLicis Pubescentis Radix).

OTHER INFORMATION:

SPL UNCLASSIFIED SECTION

• Keep unused plasters in pouch.
• Store at room temperature.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1599060camphor 3 % / menthol 5.1 % Medicated PatchPSN1
1599060camphor 0.03 MG/MG / menthol 0.051 MG/MG Medicated PatchSCD1
1599060camphor 3 % / menthol 5.1 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
16597-4873-42020-01-31C16284748780-19d75b9d0-022f-f424-e053-dadaa90a57ceLekon Herbal Patch Green

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
16597-4873-4Lekon Herbal Patch Green10 in 1 BAGPATCH101
16597-4873-4Lekon Herbal Patch Green10 g in 1 PATCHPATCH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
16597-4873LEKON HERBAL PATCH GREEN (MENTHOL,CAMPHOR) PATCH [TAIWAN THREE MAST PHARMACEUTICAL COMPANY LIMITED]1Legacy NDC, 2 package rows20150110_639105e5-3330-4cac-b904-b361ad3f6b76.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET1
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET1
MENTHOLACTIVE MOIETYL7T10EIP3A1
ACONITUM CARMICHAELII ROOTINACTIVE INGREDIENTXJ28061U1S1
ACONITUM KUSNEZOFFII ROOTINACTIVE INGREDIENT3L29I4K8KX1
AMPELOPSIS JAPONICA ROOTINACTIVE INGREDIENTO2672197TF1
ANGELICA DAHURICA ROOTINACTIVE INGREDIENT1V63N2S9721
ANGELICA PUBESCENS ROOTINACTIVE INGREDIENT0MF1EI01KJ1
ANGELICA SINENSIS ROOTINACTIVE INGREDIENTB66F4574UG1
BLETILLA STRIATA BULBINACTIVE INGREDIENT00T5SH6SEJ1
ILEX PUBESCENS ROOTINACTIVE INGREDIENTV5V22LFX731
LICORICEINACTIVE INGREDIENT61ZBX548831
LINDERA AGGREGATA ROOTINACTIVE INGREDIENT517Q7XRT2T1
NOTOPTERYGIUM FRANCHETII ROOTINACTIVE INGREDIENTKRT28P6ITK1
PAEONIA LACTIFLORA ROOTINACTIVE INGREDIENT3Z3866YW6P1
REHMANNIA GLUTINOSA ROOTINACTIVE INGREDIENT1BEM3U6LQQ1
RHEUM OFFICINALE ROOTINACTIVE INGREDIENTA47JP5ZG9M1
SALIX BABYLONICA WHOLEINACTIVE INGREDIENT629X19YOW61
SCROPHULARIA NINGPOENSIS ROOTINACTIVE INGREDIENTHC0FB6P85R1
SOPHORA FLAVESCENS ROOTINACTIVE INGREDIENTIYR6K8KQ5K1

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
16597-487316597-4873-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
66006763-1fd4-4279-8a88-f49494a0ff89639105e5-3330-4cac-b904-b361ad3f6b762014-12-29WarningsExact identifier
spl id: 66006763-1fd4-4279-8a88-f49494a0ff89
spl set id: 639105e5-3330-4cac-b904-b361ad3f6b76

Reported adverse events (FAERS/openFDA)#

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