MOGUT- lactobacillus fermentum, lactobacillus sakei, leuconostoc holzapfelii, leuconostoc mesenteroides, enterococcus faecium liquid

MOGUT by

Drug Labeling and Warnings

MOGUT by is a Otc medication manufactured, distributed, or labeled by COENBIO CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lactobacillus and Leuconostocspp. from Korean Kimchi and soybean paste

INACTIVE INGREDIENT

Persimmon vinegar(0.1%),Black soybean(0.1%), Dried broccoli sprout(0.1%), Mixed probioticsfermented liquid(99.7%)

PURPOSE

Cure chronic constipation
Diet effect
Alleviation of lactose intolerance, diarrhea, and peptic ulcer
Anti-allergic effects

Stimulation of hair growth: pilatoryeffect
Degradation of cholesterol and neutral lipid in blood vessel
Anti-oxidant effect

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

-Drinktwice a day (50ml per each time)
-Recommending drink it in the morning and night.
-It is okay to drink after eating if the person is sensible for their stomach.

WARNINGS

-Keep it in the refrigerator(4~7°C). DO NOT KEEP IT IN THE FREEZER
-Under above condition 3 months in the refrigerator but recommendtodrink it within 1 month for better taste and flavor.

DOSAGE & ADMINISTRATION

-Drinktwice a day (50ml per each time)
-Recommending drink it in the morning and night.
-It is okay to drink after eating if the person is sensible for their stomach.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOGUT 
lactobacillus fermentum, lactobacillus sakei, leuconostoc holzapfelii, leuconostoc mesenteroides, enterococcus faecium liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71682-0001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTOBACILLUS REUTERI (UNII: 9913I24QEE) (LACTOBACILLUS REUTERI - UNII:9913I24QEE)	LACTOBACILLUS REUTERI	20 g  in 100 mL
ENTEROCOCCUS FAECIUM (UNII: 34YYS7G16P) (ENTEROCOCCUS FAECIUM - UNII:34YYS7G16P)	ENTEROCOCCUS FAECIUM	20 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PERSIMMON (UNII: 4V023DD7KL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71682-0001-1	800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/01/2017

Labeler - COENBIO CO., LTD. (557838988)

Registrant - COENBIO CO., LTD. (557838988)

Establishment
Name	Address	ID/FEI	Business Operations
COENBIO CO., LTD.		557838988	pack(71682-0001) , label(71682-0001) , manufacture(71682-0001)