FDA.reportPublic FDA data

HOUKEA Foot Bath Beads

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 00:32:43

Label at a glance#

ProductHOUKEA Foot Bath Beads
Active ingredientTOCOPHEROL, LITHOSPERMUM ERYTHRORHIZON ROOT, MENTHA PIPERITA LEAF
Label structure10 sections

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

LITHOSPERMUM ERYTHRORHIZON ROOT、MENTHA PIPERITA LEAF、 TOCOPHEROL

Purpose

OTC - PURPOSE SECTION

Promote metabolism and blood circulation; relieve varicose veins; lift and tighten skin; accelerate fat decomposition

Use

OTC - WHEN USING SECTION

Take out one ofthe products and put it into a container suitable for foot soaking, and add warm water of 40-50 degrees. After the product is completely dissolved, soak your feet in it and let it stand for 15-30 minutes. After soaking, dry your feet.

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.

SAFE HANDLING WARNING 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
84660-102-01HOUKEA Foot Bath Beads10 mg in 1 BOXLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84660-102HOUKEA FOOT BATH BEADS (GLYCERIN) LIQUID [GUANGDONG XIMONTH TECHNOLOGY CO., LTD.]11 package rows20241102_25d2b6b8-79fc-5515-e063-6394a90ab9dd.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
84660-10284660-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ALLANTOIN344S277G0ZIACT
TOCOPHEROLR0ZB2556P8ACTIB
LITHOSPERMUM ERYTHRORHIZON ROOT9I70D8O47IACTIB
MENTHA PIPERITA LEAFA389O33LX6ACTIB

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
25d2b6b8-79fd-5515-e063-6394a90ab9dd25d2b6b8-79fc-5515-e063-6394a90ab9dd2024-10-31WarningsExact identifier
spl id: 25d2b6b8-79fd-5515-e063-6394a90ab9dd
spl set id: 25d2b6b8-79fc-5515-e063-6394a90ab9dd

Reported adverse events (FAERS/openFDA)#

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