FDA.reportPublic FDA data

ANTHEMIS NOBILIS

Product NDC
60512-6599
11-digit product format
605126599
Labeler code
60512
Product ID
60512-6599_e6ea7416-1dda-43a7-aeff-9ef4a065eca4
Type
HUMAN OTC DRUG
Nonproprietary name
ANTHEMIS NOBILIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CHAMOMILE
Active strength
1 [hp_X]/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-6599-12025-12-29C16284748780-19d75b9d0-afff-f424-e053-dadaa90a57ce73244a85-83ec-418e-94be-0ebe1f43ca54
60512-6599-12020-01-31C16284748780-19d75b9d0-afff-f424-e053-dadaa90a57ce73244a85-83ec-418e-94be-0ebe1f43ca54

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHAMOMILEACTIVE INGREDIENTFGL3685T2XANTHEMIS NOBILIS PELLET [HOMEOLAB USA INC.]1
CHAMOMILEACTIVE MOIETYFGL3685T2XANTHEMIS NOBILIS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANTHEMIS NOBILIS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ANTHEMIS NOBILIS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6599ANTHEMIS NOBILIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_73244a85-83ec-418e-94be-0ebe1f43ca54.zip