FDA.reportPublic FDA data

CAULOPHYLLUM THALICTROIDES

Product NDC
60512-1012
11-digit product format
605121012
Labeler code
60512
Product ID
60512-1012_afed485f-30e7-4077-9543-3d245e090a7a
Type
HUMAN OTC DRUG
Nonproprietary name
CAULOPHYLLUM THALICTROIDES
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CAULOPHYLLUM THALICTROIDES ROOT
Active strength
3 [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
60512-1012-12025-12-29C16284748780-19d75b9d0-8a46-f424-e053-dadaa90a57ce6c76692d-74bd-4245-9257-ab7852005005
60512-1012-12020-01-31C16284748780-19d75b9d0-8a46-f424-e053-dadaa90a57ce6c76692d-74bd-4245-9257-ab7852005005

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CAULOPHYLLUM THALICTROIDES ROOTACTIVE INGREDIENTJTJ6HH6YEHCAULOPHYLLUM THALICTROIDES PELLET [HOMEOLAB USA INC.]1
CAULOPHYLLUM THALICTROIDES ROOTACTIVE MOIETYJTJ6HH6YEHCAULOPHYLLUM THALICTROIDES PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCAULOPHYLLUM THALICTROIDES PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CAULOPHYLLUM THALICTROIDES PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1012CAULOPHYLLUM THALICTROIDES PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_6c76692d-74bd-4245-9257-ab7852005005.zip