NDC 15631-0136

CIMICIFUGA RACEMOSA

Cimicifuga Racemosa

CIMICIFUGA RACEMOSA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Black Cohosh.

Product ID15631-0136_a0bf1728-7704-6ba9-e053-2a95a90ad24e
NDC15631-0136
Product TypeHuman Otc Drug
Proprietary NameCIMICIFUGA RACEMOSA
Generic NameCimicifuga Racemosa
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameBLACK COHOSH
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0136-0

100 PELLET in 1 PACKAGE (15631-0136-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0136-2 [15631013602]

CIMICIFUGA RACEMOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0136-3 [15631013603]

CIMICIFUGA RACEMOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0136-1 [15631013601]

CIMICIFUGA RACEMOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0136-5 [15631013605]

CIMICIFUGA RACEMOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0136-0 [15631013600]

CIMICIFUGA RACEMOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0136-4 [15631013604]

CIMICIFUGA RACEMOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

Drug Details

Active Ingredients

IngredientStrength
BLACK COHOSH1 [hp_X]/1

OpenFDA Data

SPL SET ID:d0a9275d-cd09-44f6-9678-e1eb67d0a60d
Manufacturer
UNII

NDC Crossover Matching brand name "CIMICIFUGA RACEMOSA" or generic name "Cimicifuga Racemosa"

NDCBrand NameGeneric Name
0220-1385Cimicifuga racemosaBLACK COHOSH
0360-0128CIMICIFUGA RACEMOSACIMICIFUGA RAC.
0360-0129CIMICIFUGA RACEMOSACIMICIFUGA RAC.
15631-0136CIMICIFUGA RACEMOSACIMICIFUGA RACEMOSA
15631-0562CIMICIFUGA RACEMOSACIMICIFUGA RACEMOSA
37662-0306Cimicifuga RacemosaCimicifuga Racemosa
37662-0307Cimicifuga RacemosaCimicifuga Racemosa
37662-0308Cimicifuga RacemosaCimicifuga Racemosa
37662-0309Cimicifuga RacemosaCimicifuga Racemosa
37662-0310Cimicifuga RacemosaCimicifuga Racemosa
37662-0311Cimicifuga RacemosaCimicifuga Racemosa
37662-0312Cimicifuga RacemosaCimicifuga Racemosa
37662-0313Cimicifuga RacemosaCimicifuga Racemosa
60512-6598CIMICIFUGA RACEMOSACIMICIFUGA RACEMOSA
66096-818Cimicifuga RacemosaCIMICIFUGA RACEMOSA
68428-318Cimicifuga racemosaBLACK COHOSH
71919-200Cimicifuga racemosaBLACK COHOSH
62106-7200ACTAEA RACEMOSACIMICIFUGA RACEMOSA
69152-1081Cimicifuga racemosa 30CCimicifuga racemosa

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.