FDA.reportPublic FDA data

COCCULUS INDICUS

Product NDC
60512-6608
11-digit product format
605126608
Labeler code
60512
Product ID
60512-6608_c3ac8e12-a1a6-4174-abf5-b71a338e5bdf
Type
HUMAN OTC DRUG
Nonproprietary name
COCCULUS INDICUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ANAMIRTA COCCULUS SEED
Active strength
4 [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
60512-6608-12025-12-29C16284748780-19d75b9d0-0631-f424-e053-dadaa90a57cee33aed52-0354-4d89-a342-6c40ca8b4784
60512-6608-12020-01-31C16284748780-19d75b9d0-0631-f424-e053-dadaa90a57cee33aed52-0354-4d89-a342-6c40ca8b4784

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANAMIRTA COCCULUS SEEDACTIVE INGREDIENT810258W28UCOCCULUS INDICUS PELLET [HOMEOLAB USA INC.]1
ANAMIRTA COCCULUS SEEDACTIVE MOIETY810258W28UCOCCULUS INDICUS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCOCCULUS INDICUS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554COCCULUS INDICUS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6608COCCULUS INDICUS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_e33aed52-0354-4d89-a342-6c40ca8b4784.zip