FDA.reportPublic FDA data

TIESO FOR MAN SOOTHING CREAM (70 ml)

Manufacturer
ATEC CO., LTD. | ANDIVA Inc.
Effective date
2019-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:18:47

Label at a glance#

ProductTIESO FOR MAN SOOTHING
Active ingredientDIMETHICONE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

soothing creamsoothing cream

Active Ingredient

Dimethicone

Inactive Ingredients

Water, Propylene Glycol, Glycerin, Lepidium Meyenii Root Extract, Niacinamide, 1,2-Hexanediol, Alcohol, Snail Secretion Filtrate , Octyldodeceth-16, Arginine, Carbomer, Ammonium Acryloyldimethyltaurate/VP Copolymer, Chlorphenesin, Butylene Glycol, Sucrose Distearate , Hydroxyethylcellulose, Hydrogenated Lecithin, Glyceryl Acrylate/Acrylic Acid Copolymer, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Diospyros Kaki Leaf Extract, Morus Alba Root Extract, Disodium EDTA, Portulaca Oleracea Extract, Hyaluronic Acid, Centella Asiatica Extract, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Argania Spinosa Kernel Oil, Glycyrrhiza Glabra (Licorice) Root Extract, Hydrolyzed Collagen, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Fragrance

OTC - ACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - ASK DOCTOR/PHARMACIST SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

INACTIVE INGREDIENT SECTION

OTC - STOP USE SECTION

OTC - WHEN USING SECTION

DOSAGE & ADMINISTRATION SECTION

WARNINGS SECTION

OTHER SAFETY INFORMATION

INDICATIONS & USAGE SECTION

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
69978-070069978-0700-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OACTIB
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SUCROSE DISTEARATE33X4X4B90SIACT
ALOE VERA LEAFZY81Z83H0XIACT
DIOSPYROS KAKI LEAFQ71GF9OBNOIACT
CENTELLA ASIATICA7M867G6T1UIACT
ROSEMARYIJ67X351P9IACT
PURSLANEM6S840WXG5IACT
POLYGONUM CUSPIDATUM ROOT7TRV45YZF7IACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
LEPIDIUM MEYENII ROOTHP7119212TIACT
NIACINAMIDE25X51I8RD4IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ALCOHOL3K9958V90MIACT
OCTYLDODECETH-16RJV574G0DEIACT
ARGININE94ZLA3W45FIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CHLORPHENESINI670DAL4SZIACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
MORUS ALBA ROOTCST1G9BZGDIACT
EDETATE DISODIUM7FLD91C86KIACT
HYALURONIC ACIDS270N0TRQYIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
ARGAN OIL4V59G5UW9XIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
CHAMOMILEFGL3685T2XIACT

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
b55f729b-14a6-e96c-e053-2995a90ad4168bf67a98-9d06-5a0a-e053-2995a90af5c42020-11-30Exact identifier
spl set id: 8bf67a98-9d06-5a0a-e053-2995a90af5c4

Reported adverse events (FAERS/openFDA)#

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