TIESO FOR MAN SOOTHING CREAM (70 ml)

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 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73184-0700-12021-10-22C16284748780-1c7ccaba7-18ed-fd44-e053-dadaa90aa01bTIESO FOR MAN SOOTHING CREAM (70 ml)
73184-0700-12021-07-23C16284748780-1c7ccaba7-18ed-fd44-e053-dadaa90aa01bTIESO FOR MAN SOOTHING CREAM (70 ml)

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
73184-070073184-0700-1

Ingredients#

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

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

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
ceea202d-472e-7ae7-e053-2995a90acd11b4c2c2f6-ac4f-5b47-e053-2a95a90a33a02021-10-22Exact identifier
spl set id: b4c2c2f6-ac4f-5b47-e053-2a95a90a33a0

Reported adverse events (FAERS/openFDA)#

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