FDA.reportPublic FDA data

Aesculus

Product NDC
53645-1370
11-digit product format
536451370
Labeler code
53645
Product ID
53645-1370_f0315d99-dba3-c57f-e053-2a95a90a943e
Type
HUMAN OTC DRUG
Nonproprietary name
Aesculus
Dosage form
GLOBULE
Route
ORAL
Labeler
True Botanica, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-12-29
Marketing end
0000-00-00
Substance
AESCULUS HIPPOCASTANUM WHOLE
Active strength
50 [hp_X]/23g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct53645-1370DDiscontinued by firm2026-08-11
excluded packagepackage53645-137053645-1370-2DDiscontinued by firm2026-08-11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53645-1370-22021-01-31C16284748780-1ba0f9c33-542c-a910-e053-dadaa90a0b85Aesculus 50x
53645-1370-22021-01-29C16284748780-1ba0f9c33-542c-a910-e053-dadaa90a0b85Aesculus 50x

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-1370AESCULUS GLOBULE [TRUE BOTANICA, LLC]5Legacy NDC20230502_6190e9c0-2dda-6d16-e053-2a91aa0ae5cc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53645-1370-25364513700223 g in 1 BOTTLE (53645-1370-2) 23 g2017-12-290000-00-00NoNoCurrent