FDA.reportPublic FDA data

CIMICIFUGA RACEMOSA

Product NDC
60512-6598
11-digit product format
605126598
Labeler code
60512
Product ID
60512-6598_d95b1a8c-20bc-4887-83b4-ab8bff08f8cf
Type
HUMAN OTC DRUG
Nonproprietary name
CIMICIFUGA RACEMOSA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ACTAEA CIMICIFUGA ROOT
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
60512-6598-12025-12-29C16284748780-19d75b9d0-30dc-f424-e053-dadaa90a57cea0dbb312-7777-4377-ba86-6f0323f8cda3
60512-6598-12020-01-31C16284748780-19d75b9d0-30dc-f424-e053-dadaa90a57cea0dbb312-7777-4377-ba86-6f0323f8cda3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACTAEA CIMICIFUGA ROOTACTIVE INGREDIENT65J267BAZTCIMICIFUGA RACEMOSA PELLET [HOMEOLAB USA INC.]1
ACTAEA CIMICIFUGA ROOTACTIVE MOIETY65J267BAZTCIMICIFUGA RACEMOSA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCIMICIFUGA RACEMOSA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CIMICIFUGA RACEMOSA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6598CIMICIFUGA RACEMOSA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_a0dbb312-7777-4377-ba86-6f0323f8cda3.zip