FDA.reportPublic FDA data

CANTHARIS

Product NDC
60512-9151
11-digit product format
605129151
Labeler code
60512
Product ID
60512-9151_bf3ee20b-6d71-4ed3-8de2-a0df5a4a8961
Type
HUMAN OTC DRUG
Nonproprietary name
CANTHARIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-30
Marketing end
0000-00-00
Substance
LYTTA VESICATORIA
Active strength
3 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-9151-12025-12-28C16284748780-19d75b9d0-30fa-f424-e053-dadaa90a57ce32c40d50-2c2c-4e13-b325-1f161607b59a
60512-9151-12020-01-31C16284748780-19d75b9d0-30fa-f424-e053-dadaa90a57ce32c40d50-2c2c-4e13-b325-1f161607b59a

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LYTTA VESICATORIAACTIVE INGREDIENT3Q034RO3BTCANTHARIS PELLET [HOMEOLAB USA INC]1
LYTTA VESICATORIAACTIVE MOIETY3Q034RO3BTCANTHARIS PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCANTHARIS PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554CANTHARIS PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-9151CANTHARIS PELLET [HOMEOLAB USA INC]1Legacy NDC20111205_32c40d50-2c2c-4e13-b325-1f161607b59a.zip