HOUKEA Wormwood Foot Patch

Manufacturer
Guangdong Ximonth Technology Co., Ltd.
Effective date
2024-10-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:32:40

Label at a glance#

ProductHOUKEA Wormwood Foot Patch
Active ingredientMENTHA PIPERITA LEAF, ARTEMISIA VULGARIS ROOT, TOCOPHEROL
Label structure10 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

ARTEMISIA VULGARIS ROOT、MENTHA PIPERITA LEAF、TOCOPHEROL

Purpose

OTC - PURPOSE SECTION

Reduce liver burden; improve sleep quality; relieve stress and fatigue; enhance the joy of life

Use

OTC - WHEN USING SECTION

Clean the soles of your feet and keep them dry. Apply a piece of this product to the soles of your feet and press gently to ensure it sticks. Leave it on for 6-8 hours and then tear it off.

Warnings

WARNINGS SECTION

Please keep out of reach of children.Do not swallow.Please clean your hands before use to ensure the best results from the product.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place.

Do not use

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

Stop Use

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children. Do not swallow.

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

GLYCERIN、ALLANTOIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84660-099-01HOUKEA Wormwood Foot Patch12 mg in 1 BOXPATCH121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84660-099HOUKEA WORMWOOD FOOT PATCH (GLYCERIN) PATCH [GUANGDONG XIMONTH TECHNOLOGY CO., LTD.]11 package rows20241102_25d1ec70-7e62-ccc2-e063-6394a90a4463.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84660-09984660-099-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
25d1ec70-7e63-ccc2-e063-6394a90a446325d1ec70-7e62-ccc2-e063-6394a90a44632024-10-31WarningsExact identifier
spl id: 25d1ec70-7e63-ccc2-e063-6394a90a4463
spl set id: 25d1ec70-7e62-ccc2-e063-6394a90a4463

Reported adverse events (FAERS/openFDA)#

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