FDA.reportPublic FDA data

Shengguxiang Foot Care Bath Liquid

Manufacturer
Shandong Shengguxiang Health Management Co., Ltd
Effective date
2021-10-19
Label type
HUMAN OTC DRUG LABEL
Version
32749
Source
full-release
Hydrated at
2026-05-31 23:44:20

Label at a glance#

ProductShengguxiang Foot Care Bath Liquid
Active ingredientMENTHOL
Label structure9 sections

Dosage and administration

Take 1-2 bags of this product and mix with 6.6 lbs (3 kg) of 212°F (100℃) water, and then add an appropriate amount of cold water. Soak your feet for 15-20 minutes at a water temperature of about 104°F (40°) until the body sweats slightly. Long-term use is recommended. .

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol      1%

Purpose

OTC - PURPOSE SECTION

Menthol 1%     Skin Protectant

Use

INDICATIONS & USAGE SECTION

Home foot bath. Beauty spa club, health care center and foot bath experience shop.

Warning

WARNINGS SECTION

  • This product is forbidden for patients with heart bypass or stents.
  • This product is forbidden for critically ill patients and cancer patients.
  • This product is forbidden for parturient women.
  • This product is forbidden for patients with internal or external bleeding and subcutaneous hemorrhage.
  • This product is forbidden for severe diabetic patients (severe skin ulceration), cardiovascular and cerebrovascular patients, severely hypertensive patients.
  • For women who are allergic to Chinese herbal medicine during menstruation, use it with caution.
  • This product is only for foot bathing and foot health care.
  • External use only.

Directions

DOSAGE & ADMINISTRATION SECTION

Take 1-2 bags of this product and mix with 6.6 lbs (3 kg) of 212°F (100℃) water, and then add an appropriate amount of cold water. Soak your feet for 15-20 minutes at a water temperature of about 104°F (40°) until the body sweats slightly. Long-term use is recommended. .

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop using the product if you are allergic or have adverse effect.

Manufactured by Shandong Shengguxiang Health Management Co, LtdNo.27-1, Hexiangju Community, Bazi Village, Hehua Road Street, Licheng District, Jinan, Shandong 250108, ChinaProduct of China

SPL UNCLASSIFIED SECTION

Distributed by Bravo Home Products, Inc
                     2425 Lee Ave, South El Monte, CA 91733

Inactive Ingredients

INACTIVE INGREDIENT SECTION

ACORUS CALAMUS ROOT, RHINACANTHUS NASUTUS WHOLE, SOPHORA FLAVESCENS ROOT, CARTHAMUS TINCTORIUS WHOLE, ZINGIBER OFFICINALE WHOLE, SPATHOLOBUS SUBERECTUS STEM, BUPLEURUM CHINENSE ROOT, LEONURUS JAPONICUS STEM, SALVIA MILTIORRHIZA ROOT, MORINGA OLEIFERA SEED OIL, ANGELICA SINENSIS ROOT, FALLOPIA MULTIFLORA ROOT, RHODIOLA ROSEA ROOT, SAUSSUREA INVOLUCRATA, LIQUIDAMBAR FORMOSANA FRUIT, ALBIZIA JULIBRISSIN BARK, WOLFIPORIA COCOS WHOLE, GLYCYRRHIZA URALENSIS ROOT, ARTEMISIA ARGYI LEAF, SCHISANDRA CHINENSIS FRUIT, CINNAMOMUM CASSIA TWIG, DICTAMNUS DASYCARPUS ROOT BARK, ZIZIPHUS JUJUBA VAR. SPINOSA SEED, ZANTHOXYLUM BUNGEANUM FRUIT, LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT, PANAX QUINQUEFOLIUS WHOLE, POLYSORBATE 80, CARAMEL COLOR, SODIUM BENZOATE, WATER

Drug Facts Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308942menthol 1 % Topical SolutionPSN32749
308942menthol 10 MG/ML Topical SolutionSCD32749
308942menthol 1 % Topical SolutionSY32749

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81981-001-222023-01-30C16284748780-1f386c649-db36-0266-e053-dadaa90a7c1aShandong Shengguxiang Health Management Co., Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81981-001-22Shengguxiang Foot Care Bath Liquid22 mL in 1 PACKETLIQUID2232749
81981-001-22Shengguxiang Foot Care Bath Liquid30 in 1 PACKAGELIQUID3032749

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81981-001SHENGGUXIANG FOOT CARE BATH LIQUID (MENTHOL) LIQUID [SHANDONG SHENGGUXIANG HEALTH MANAGEMENT CO., LTD]32749Legacy NDC, 2 package rows20211020_c0c9aaff-c8ae-4121-9869-e0e90f5f0ae9.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81981-00181981-001-22

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
ACORUS CALAMUS ROOTXY1K7KIQ0FIACT
RHINACANTHUS NASUTUS WHOLEQW70YFP724IACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
CARTHAMUS TINCTORIUS WHOLE5EMV416J82IACT
ZINGIBER OFFICINALE WHOLEIN6Q3S3414IACT
SPATHOLOBUS SUBERECTUS STEMN51VZ363BAIACT
BUPLEURUM CHINENSE ROOTBMA22623YKIACT
LEONURUS JAPONICUS STEMVZZ2YX7298IACT
SALVIA MILTIORRHIZA ROOT1693AM5SBNIACT
MORINGA OLEIFERA SEED OILREM6A5QMC0IACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
FALLOPIA MULTIFLORA ROOTAUZ3VD75MCIACT
RHODIOLA ROSEA ROOT3S5ITS5ULNIACT
SAUSSUREA INVOLUCRATA FLOWERING TOP65D06L9K7FIACT
LIQUIDAMBAR FORMOSANA FRUIT7H2JA3MO62IACT
ALBIZIA JULIBRISSIN BARK0J9G6W44DVIACT
WOLFIPORIA COCOS WHOLEY1I7Z6FF4RIACT
GLYCYRRHIZA URALENSIS ROOT42B5YD8F0KIACT
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT
SCHISANDRA CHINENSIS FRUITABS794681CIACT
CINNAMOMUM CASSIA TWIG4UD6VQR2UPIACT
DICTAMNUS DASYCARPUS ROOT BARKLA97176ILSIACT
ZIZIPHUS JUJUBA VAR. SPINOSA SEEDS50MZ3Y08RIACT
ZANTHOXYLUM BUNGEANUM FRUIT3CIP16A418IACT
LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOTRR83T99U97IACT
PANAX QUINQUEFOLIUS WHOLE0P067WOA1XIACT
POLYSORBATE 806OZP39ZG8HIACT
CARAMELT9D99G2B1RIACT
SODIUM BENZOATEOJ245FE5EUIACT
WATER059QF0KO0RIACT

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
252d7be1-68c6-4139-8a1a-98cc7fd9aa4ec0c9aaff-c8ae-4121-9869-e0e90f5f0ae92021-10-19WarningsExact identifier
spl id: 252d7be1-68c6-4139-8a1a-98cc7fd9aa4e
spl set id: c0c9aaff-c8ae-4121-9869-e0e90f5f0ae9

Reported adverse events (FAERS/openFDA)#

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