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  5. NDC Package Code: 71682-0001-1 Mogut

NDC Package 71682-0001-1 Mogut

Lactobacillus Fermentum,Lactobacillus Sakei,Leuconostoc Holzapfelii,Leuconostoc - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
71682-0001-1
Package Description:
800 mL in 1 BOTTLE, PLASTIC
Product Code:
71682-0001
Proprietary Name:
Mogut
Non-Proprietary Name:
Lactobacillus Fermentum, Lactobacillus Sakei, Leuconostoc Holzapfelii, Leuconostoc Mesenteroides, Enterococcus Faecium
Substance Name:
Enterococcus Faecium; Lactobacillus Reuteri
Usage Information:
-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.
11-Digit NDC Billing Format:
71682000101
Product Type:
Human Otc Drug
Labeler Name:
Coenbio Co., Ltd.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ENTEROCOCCUS FAECIUM 20 g/100mL
  • LACTOBACILLUS REUTERI 20 g/100mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    08-01-2017
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71682-0001-1?

    The NDC Packaged Code 71682-0001-1 is assigned to a package of 800 ml in 1 bottle, plastic of Mogut, a human over the counter drug labeled by Coenbio Co., Ltd.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 71682-0001 included in the NDC Directory?

    Yes, Mogut with product code 71682-0001 is active and included in the NDC Directory. The product was first marketed by Coenbio Co., Ltd. on August 01, 2017 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71682-0001-1?

    The 11-digit format is 71682000101. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-171682-0001-15-4-271682-0001-01