FDA.reportPublic FDA data

Legere Eucalyptus Foot Patch

Manufacturer
Myriad Co., Ltd.
Effective date
2022-12-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:52:46

Label at a glance#

ProductLegere Eucalyptus Foot Patch
Active ingredientSTARCH, CORN
Label structure11 sections

Indications and uses

May help relieve minor aches and pain

Dosage and administration

Adults and children 4 years of age and over: Step 1: Clean and dry area for the patch to be attached. Step 2: Remove the protective cover sheet and gently apply. Step 3: Leave it on at least 4hours before remove. Children under 4years of age: Consult with a doctor.

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Skin Protectant

Uses

DOSAGE & ADMINISTRATION SECTION

May help relieve minor aches and pain

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Topical Starch 31.58%

Warnings

WARNINGS SECTION

For external use only / Don’t eat or swallow it

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

When using this product

OTC - WHEN USING SECTION

■ Do not use otherwise than directed.

■ Do not stretch out the adhesive tape.

■ Do not take out the contents from the patch.

■ If the patch has been ripped, discard it immediately.

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ If allergic reaction or irritation occurs

■ If you are pregnant, nursing or under medial treatment

Warnings

OTC - DO NOT USE SECTION

■ On wounds, damaged skin, or face.

■ If you are allergic to any ingredients of this product.

■ With, or at the same time as, other external products.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Bamboo vinegar, Tourmaline, Eucalyptus oil, Mugwort extract, Loquat extract, Vitamin C, Highly purified silica, Perlite, Polyhydric alcohol

directions

INDICATIONS & USAGE SECTION

Adults and children 4 years of age and over:

Step 1: Clean and dry area for the patch to be attached.

Step 2: Remove the protective cover sheet and gently apply.

Step 3: Leave it on at least 4hours before remove.

Children under 4years of age: Consult with a doctor.

Légère Eucalyptus Foot Patch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82504-103-01

8250482504

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82504-103-012024-01-30C16284748780-11030e365-2bab-111a-e063-dadaa90a10e2Légère Eucalyptus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82504-103-01Legere Eucalyptus Foot Patch40 g in 1 BOXPATCH403

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82504-103LEGERE EUCALYPTUS FOOT PATCH (TOPICAL STARCH) PATCH [MYRIAD CO., LTD.]3Legacy NDC, 1 package rows20221230_d55c2fe9-85bf-01f8-e053-2995a90a4d19.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82504-10382504-103-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
VANILLYL BUTYL ETHERS2ULN37C9RIACT
PERLITE0SG101ZGK9IACT
ASCORBIC ACIDPQ6CK8PD0RIACT
EUCALYPTUS OIL2R04ONI662IACT
POLIGLUSAM82LKS4QV2YIACT
STARCH, CORNO8232NY3SJACTIB
ARTEMISIA PRINCEPS LEAFSY077EW02GIACT
ERIOBOTRYA JAPONICA LEAFZ02066SV11IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
SCHORL TOURMALINE173O8XLY6TIACT
SORBITOL506T60A25RIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PYROLIGNEOUS ACIDN4G9GAT76CIACT

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
f1022a09-9d0e-3be1-e053-2a95a90aba0cd55c2fe9-85bf-01f8-e053-2995a90a4d192022-12-29WarningsExact identifier
spl id: f1022a09-9d0e-3be1-e053-2a95a90aba0c
spl set id: d55c2fe9-85bf-01f8-e053-2995a90a4d19

Reported adverse events (FAERS/openFDA)#

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