MOGUT
- Product NDC
- 71682-0001
- 11-digit product format
- 716820001
- Labeler code
- 71682
- Product ID
- 71682-0001_9bff4c2b-6abe-1194-e053-2995a90a2ca5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lactobacillus fermentum, Lactobacillus sakei, Leuconostoc holzapfelii, Leuconostoc mesenteroides, Enterococcus faecium
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- COENBIO CO., LTD.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-08-01
- Marketing end
- 0000-00-00
- Substance
- LACTOBACILLUS REUTERI; ENTEROCOCCUS FAECIUM
- Active strength
- 20 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71682-0001-1 | MOGUT | 800 mL in 1 BOTTLE, PLASTIC | LIQUID | 800 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71682-0001 | MOGUT (LACTOBACILLUS FERMENTUM, LACTOBACILLUS SAKEI, LEUCONOSTOC HOLZAPFELII, LEUCONOSTOC MESENTEROIDES, ENTEROCOCCUS FAECIUM) LIQUID [COENBIO CO., LTD.] | 2 | Legacy NDC, 1 package rows | 20200113_57ca4c0b-1ce9-13bd-e053-2991aa0a6d8d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71682-0001-1 | 71682000101 | 800 mL in 1 BOTTLE, PLASTIC (71682-0001-1) | 800 ml | 2017-08-01 | 0000-00-00 | No | No | Current |