Drug Facts

MOGUT- lactobacillus fermentum, lactobacillus sakei, leuconostoc holzapfelii, leuconostoc mesenteroides, enterococcus faecium liquid
COENBIO CO., LTD.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

Lactobacillus and Leuconostocspp. from Korean Kimchi and soybean paste

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

•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 the children

-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.

-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.

-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.

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

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

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

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

Labeler - COENBIO CO., LTD. (557838988)

Registrant - COENBIO CO., LTD. (557838988)

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