TIESO RAPIDO- menthol, benzalkonium chloride cream

TIESO RAPIDO by

Drug Labeling and Warnings

TIESO RAPIDO 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 Ingredients Purposes

Menthol 0.1 %.....................................external analgesic
Benzalkonium chloride 0.04 %...........antibacterial

Inactive ingredients

Water, Alcohol, Triolein, Ethylhexyl Stearate, Lepidium Meyenii Root
Extract, 1,2-Hexanediol, Caprylyl Methicone, Glycerin, Fragrance, Methyl Glucose Sesquistearate, Acrylates/Beheneth-25 Methacrylate Copolymer, Portulaca Oleracea Extract, Xylitylglucoside, Sorbitan Stearate, Anhydroxylitol, Butylene Glycol, Xylitol, Carbomer, Disodium EDTA, Tromethamine, Glucose

INGREDIENTS AND APPEARANCE

TIESO RAPIDO 
menthol, benzalkonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69978-0080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.08 g  in 80 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.032 g  in 80 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
GLYCERYL TRIOLEATE (UNII: O05EC62663)
LEPIDIUM MEYENII ROOT (UNII: HP7119212T)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
GLYCERIN (UNII: PDC6A3C0OX)
XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
ANHYDROXYLITOL (UNII: 8XWR7NN42F)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
TROMETHAMINE (UNII: 023C2WHX2V)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)
PURSLANE (UNII: M6S840WXG5)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
XYLITOL (UNII: VCQ006KQ1E)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69978-0080-1	1 in 1 BOX	09/10/2019
1		80 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 not final	part333A	09/10/2019

Labeler - ATEC CO., LTD. (689276681)

Registrant - ANDIVA Inc. (689276681)

Establishment
Name	Address	ID/FEI	Business Operations
ATEC CO., LTD.		689276681	manufacture(69978-0080)