[de-listing] TIESO FOR MAN MALE CLEANSER (4 ml)

TIESO FOR MAN MALE CLEANSER by

Drug Labeling and Warnings

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

Drug Details [pdf]

TIESO FOR MAN MALE CLEANSER- menthol liquid 
ANDIVA Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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[de-listing] TIESO FOR MAN MALE CLEANSER (4 ml)

TIESO FOR MAN MALE CLEANSER 
menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73184-0040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.002 g  in 4 mL

Inactive Ingredients
Ingredient Name	Strength
OCTYLDODECETH-16 (UNII: RJV574G0DE)
HYALURONIC ACID (UNII: S270N0TRQY)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DIOSPYROS KAKI LEAF (UNII: Q71GF9OBNO)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
LEPIDIUM MEYENII ROOT (UNII: HP7119212T)
CHAMOMILE (UNII: FGL3685T2X)
WATER (UNII: 059QF0KO0R)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ROSEMARY (UNII: IJ67X351P9)
LAURYL HYDROXYSULTAINE (UNII: 176KKP31OZ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
XANTHAN GUM (UNII: TTV12P4NEE)
PURSLANE (UNII: M6S840WXG5)
ARGININE (UNII: 94ZLA3W45F)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
MORUS ALBA ROOT (UNII: CST1G9BZGD)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ALCOHOL (UNII: 3K9958V90M)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73184-0040-1	4 mL in 1 POUCH; Type 0: Not a Combination Product	08/21/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/21/2019	10/22/2021

Labeler - ANDIVA Inc. (695032533)

Registrant - ANDIVA Inc. (695032533)

Establishment
Name	Address	ID/FEI	Business Operations
ATEC CO., LTD.		689276681	manufacture(73184-0040)

Revised: 10/2021

Document Id: ceea1484-54ea-3ac7-e053-2a95a90adaf0

34390-5

Set id: b4c2a38a-dfd7-7faf-e053-2995a90abd6f

Version: 2

Effective Time: 20211022