FDA.reportPublic FDA data

Baekcho-DS

Product NDC
72988-0009
11-digit product format
729880009
Labeler code
72988
Product ID
72988-0009_859906f4-7ada-e41f-e053-2a91aa0ab1b8
Type
HUMAN OTC DRUG
Nonproprietary name
Licorice Ext
Dosage form
SYRUP
Route
ORAL
Labeler
Lydia Co., Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-03-23
Marketing end
0000-00-00
Substance
LICORICE
Active strength
10 g/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72988-0009-12025-11-20C16284748780-1ba0f9c33-57ea-a910-e053-dadaa90a0b85859906f4-7ad9-e41f-e053-2a91aa0ab1b8
72988-0009-12021-01-29C16284748780-1ba0f9c33-57ea-a910-e053-dadaa90a0b85859906f4-7ad9-e41f-e053-2a91aa0ab1b8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0009BAEKCHO-DS (LICORICE EXT) SYRUP [LYDIA CO., LTD.]1Legacy NDC20190403_859906f4-7ad9-e41f-e053-2a91aa0ab1b8.zip