FDA.reportPublic FDA data

TIESO FOR MAN MALE CLEANSER

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 FOR MAN MALE CLEANSER
Active ingredientMENTHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cleansercleanser

Active Ingredient

Menthol

Inactive Ingredients

Water, Glycerin, Lepidium Meyenii Root Extract,1,2-Hexanediol, Alcohol, Lauryl Hydroxysultaine, Decyl Glucoside, Xanthan Gum, Octyldodeceth-16, Sodium Chloride, Hydroxyethylcellulose, Butylene Glycol, Portulaca Oleracea Extract, Arginine, Chlorhexidine Digluconate, Citric acid, Disodium EDTA, Hyaluronic Acid, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Diospyros Kaki Leaf Extract, Morus Alba Root Extract, Centella Asiatica Extract, Polygonum Cuspidatum Root Extract,
Scutellaria Baicalensis Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract,
Rosmarinus Officinalis (Rosemary) Leaf Extract, Fragrance

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

OTC - WHEN USING SECTION

DOSAGE & ADMINISTRATION SECTION

WARNINGS SECTION

OTHER SAFETY INFORMATION

INDICATIONS & USAGE SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73184-1200-12021-10-22C16284748780-1c7ccaba7-11f1-fd44-e053-dadaa90aa01bTIESO FOR MAN MALE CLEANSER (120 ml)
73184-1200-12021-07-23C16284748780-1c7ccaba7-11f1-fd44-e053-dadaa90aa01bTIESO FOR MAN MALE CLEANSER (120 ml)

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73184-120073184-1200-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
MORUS ALBA ROOTCST1G9BZGDIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LEPIDIUM MEYENII ROOTHP7119212TIACT
LAURYL HYDROXYSULTAINE176KKP31OZIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
XANTHAN GUMTTV12P4NEEIACT
OCTYLDODECETH-16RJV574G0DEIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYALURONIC ACIDS270N0TRQYIACT
ALOE VERA LEAFZY81Z83H0XIACT
DIOSPYROS KAKI LEAFQ71GF9OBNOIACT
CENTELLA ASIATICA7M867G6T1UIACT
POLYGONUM CUSPIDATUM ROOT7TRV45YZF7IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ALCOHOL3K9958V90MIACT
SODIUM CHLORIDE451W47IQ8XIACT
PURSLANEM6S840WXG5IACT
ARGININE94ZLA3W45FIACT
CHLORHEXIDINE GLUCONATEMOR84MUD8EIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
CHAMOMILEFGL3685T2XIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
ROSEMARYIJ67X351P9IACT
MENTHOLL7T10EIP3AACTIB

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
ceea01a2-e6fa-9948-e053-2995a90a9e26b4c2bd7d-cf0f-50b8-e053-2a95a90a2fbd2021-10-22Exact identifier
spl set id: b4c2bd7d-cf0f-50b8-e053-2a95a90a2fbd

Reported adverse events (FAERS/openFDA)#

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