NDC 15631-0378

RUMEX CRISPUS

Rumex Crispus

RUMEX CRISPUS 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 Rumex Crispus Root.

Product ID15631-0378_3528b0af-6fe0-4eca-aea8-416ddf06d63b
NDC15631-0378
Product TypeHuman Otc Drug
Proprietary NameRUMEX CRISPUS
Generic NameRumex Crispus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameRUMEX CRISPUS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0378-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0378-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0378-4 [15631037804]

RUMEX CRISPUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0378-5 [15631037805]

RUMEX CRISPUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0378-2 [15631037802]

RUMEX CRISPUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0378-0 [15631037800]

RUMEX CRISPUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0378-1 [15631037801]

RUMEX CRISPUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0378-3 [15631037803]

RUMEX CRISPUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
RUMEX CRISPUS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:f1ade3fb-c4be-44bf-b2f0-f92a574fef03
Manufacturer
UNII

NDC Crossover Matching brand name "RUMEX CRISPUS" or generic name "Rumex Crispus"

NDCBrand NameGeneric Name
0220-4435Rumex crispusRUMEX CRISPUS ROOT
0220-4454Rumex crispusRUMEX CRISPUS ROOT
0220-4455Rumex crispusRUMEX CRISPUS ROOT
0220-4456Rumex crispusRUMEX CRISPUS ROOT
0220-4457Rumex crispusRUMEX CRISPUS ROOT
0220-4458Rumex crispusRUMEX CRISPUS ROOT
0220-4459Rumex crispusRUMEX CRISPUS ROOT
15631-0378RUMEX CRISPUSRUMEX CRISPUS
15631-0672RUMEX CRISPUSRUMEX CRISPUS
37662-2001Rumex CrispusRumex Crispus
37662-2002Rumex CrispusRumex Crispus
37662-2003Rumex CrispusRumex Crispus
37662-2004Rumex CrispusRumex Crispus
37662-2005Rumex CrispusRumex Crispus
37662-2006Rumex CrispusRumex Crispus
37662-2007Rumex CrispusRumex Crispus
37662-2008Rumex CrispusRumex Crispus
37662-2009Rumex CrispusRumex Crispus
62106-8802RUMEX CRISPUSYellow dock
68428-608Rumex CrispusRumex Crispus
71919-593Rumex crispusRumex crispus
49643-406Dock, Yellow PollenRumex crispus
22840-1315Yellow Curly DockRumex crispus
22840-1316Yellow Curly DockRumex crispus
22840-1317Yellow Curly DockRumex crispus
22840-1318Yellow Curly DockRumex crispus
22840-5305Yellow Curly DockRumex crispus

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