NDC 15631-0672

RUMEX CRISPUS

Rumex Crispus

RUMEX CRISPUS is a Oral Tablet 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 ID15631-0672_ec0bc9f2-abfb-4753-92e5-9e1fb894aef6
NDC15631-0672
Product TypeHuman Otc Drug
Proprietary NameRUMEX CRISPUS
Generic NameRumex Crispus
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
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 15631-0672-3

100 TABLET in 1 CONTAINER (15631-0672-3)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0672-7 [15631067207]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0672-3 [15631067203]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0672-6 [15631067206]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0672-4 [15631067204]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0672-0 [15631067200]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0672-1 [15631067201]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0672-2 [15631067202]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0672-5 [15631067205]

RUMEX CRISPUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
RUMEX CRISPUS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:96d54449-3254-4844-8405-04b3282c690f
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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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