FDA.reportPublic FDA data

TIESO FOOT (Foot spray) : 69978-0169-1

Manufacturer
ANDIVA Inc. | ATEC Co., Ltd.
Effective date
2020-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:05:56

Label at a glance#

ProductTIESO FOOT
Active ingredientMENTHOL, BENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TIESO FOOTTIESO FOOT

Active ingredients Purposes

Benzalkonium chloride 0.04%..........Antibacterial
Menthol 0.1%.....................................Antipruritic

Inactive ingredients Water, Alcohol, Ethylhexyl
Stearate, Triolein, Lepidium Meyenii Root Extract,
1,2-Hexanediol, Caprylyl Methicone, Glycerin,
Fragrance, Glyceryl Dioleate, Methyl Glucose
Sesquistearate, Portulaca Oleracea Extract,
Xylitylglucoside, Acrylates/Beheneth-25
Methacrylate Copolymer, Sorbitan Stearate,
Anhydroxylitol, Butylene Glycol, Xylitol, Carbomer,
Disodium EDTA, Tromethamine, Glucose

OTC - ACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

OTC - WHEN USING SECTION

INACTIVE INGREDIENT SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

INDICATIONS & USAGE SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73184-0169-12021-10-22C16284748780-1c7ccaba7-11ee-fd44-e053-dadaa90aa01bTIESO FOOT (Foot spray) : 69978-0169-1
73184-0169-12021-07-23C16284748780-1c7ccaba7-11ee-fd44-e053-dadaa90aa01bTIESO FOOT (Foot spray) : 69978-0169-1

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73184-016973184-0169-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
WATER059QF0KO0RIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
LEPIDIUM MEYENII ROOTHP7119212TIACT
GLYCERINPDC6A3C0OXIACT
PURSLANEM6S840WXG5IACT
ALCOHOL3K9958V90MIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ANHYDROXYLITOL8XWR7NN42FIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
XYLITOLVCQ006KQ1EIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROMETHAMINE023C2WHX2VIACT
BEHENETH-250G17KJ5M7PIACT
SORBITAN MONOSTEARATENVZ4I0H58XIACT
EDETATE DISODIUM7FLD91C86KIACT
XYLITYLGLUCOSIDEO0IEZ166FBIACT
METHYL GLUCOSE SESQUISTEARATEV1YW10H14DIACT
GLYCERYL TRIOLEATEO05EC62663IACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
GLYCERYL DIOLEATEZ3MP1W91CWIACT
MENTHOLL7T10EIP3AACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ceea1d4d-4d24-3acf-e053-2a95a90ac2c0b4c2a81b-c0bf-50b6-e053-2a95a90a4d7a2021-10-22Exact identifier
spl set id: b4c2a81b-c0bf-50b6-e053-2a95a90a4d7a

Reported adverse events (FAERS/openFDA)#

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