Cimicifuga racemosa 30C

Product NDC
69152-1081
11-digit product format
691521081
Labeler code
69152
Product ID
69152-1081_2f2e2220-6fc8-0e0a-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Cimicifuga racemosa
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-28
Marketing end
0000-00-00
Substance
BLACK COHOSH
Active strength
30 [hp_C]/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1081-12020-01-31C16284748780-19d75b9d0-7846-f424-e053-dadaa90a57ce17216cd9-c3b5-0849-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1081-1Cimicifuga racemosa 30C96 in 1 BOTTLEPELLET966

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1081CIMICIFUGA RACEMOSA 30C (CIMICIFUGA RACEMOSA) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]6Legacy NDC, 1 package rows20160329_17216cd9-c3b5-0849-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1081-16915210810196 in 1 BOTTLEHistorical