TIESO FOR MAN SOOTHING- dimethicone cream

TIESO FOR MAN SOOTHING by

Drug Labeling and Warnings

TIESO FOR MAN SOOTHING by is a Otc medication manufactured, distributed, or labeled by ATEC CO., LTD., ANDIVA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

TIESO FOR MAN SOOTHING 
dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69978-0700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	0.77 g  in 70 mL

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SUCROSE DISTEARATE (UNII: 33X4X4B90S)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIOSPYROS KAKI LEAF (UNII: Q71GF9OBNO)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
ROSEMARY (UNII: IJ67X351P9)
PURSLANE (UNII: M6S840WXG5)
POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
LEPIDIUM MEYENII ROOT (UNII: HP7119212T)
NIACINAMIDE (UNII: 25X51I8RD4)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ALCOHOL (UNII: 3K9958V90M)
OCTYLDODECETH-16 (UNII: RJV574G0DE)
ARGININE (UNII: 94ZLA3W45F)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CHLORPHENESIN (UNII: I670DAL4SZ)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MORUS ALBA ROOT (UNII: CST1G9BZGD)
EDETATE DISODIUM (UNII: 7FLD91C86K)
HYALURONIC ACID (UNII: S270N0TRQY)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
ARGAN OIL (UNII: 4V59G5UW9X)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
CHAMOMILE (UNII: FGL3685T2X)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69978-0700-1	1 in 1 BOX	07/04/2019
1		70 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	07/04/2019

Labeler - ATEC CO., LTD. (689276681)

Registrant - ANDIVA Inc. (695032533)

Establishment
Name	Address	ID/FEI	Business Operations
ATEC CO., LTD.		689276681	manufacture(69978-0700)