NDC 15631-0578

EQUISETUM HYEMALE

Equisetum Hyemale

EQUISETUM HYEMALE 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 Equisetum Hyemale.

Product ID15631-0578_2237ea37-78bc-4827-9985-725ac6c4b21e
NDC15631-0578
Product TypeHuman Otc Drug
Proprietary NameEQUISETUM HYEMALE
Generic NameEquisetum Hyemale
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 NameEQUISETUM HYEMALE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0578-1

4 TABLET in 1 BLISTER PACK (15631-0578-1)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0578-1 [15631057801]

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

NDC 15631-0578-3 [15631057803]

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

NDC 15631-0578-5 [15631057805]

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

NDC 15631-0578-6 [15631057806]

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

NDC 15631-0578-7 [15631057807]

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

NDC 15631-0578-0 [15631057800]

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

NDC 15631-0578-2 [15631057802]

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

NDC 15631-0578-4 [15631057804]

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

Drug Details

Active Ingredients

IngredientStrength
EQUISETUM HYEMALE3 [hp_X]/1

OpenFDA Data

SPL SET ID:53253d9b-6ac7-4880-93b4-011d32499b85
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "EQUISETUM HYEMALE" or generic name "Equisetum Hyemale"

    NDCBrand NameGeneric Name
    0220-1885Equisetum hyemaleEQUISETUM HYEMALE
    0220-1886Equisetum hyemaleEQUISETUM HYEMALE
    0220-1889Equisetum hyemaleEQUISETUM HYEMALE
    0220-1890Equisetum hyemaleEQUISETUM HYEMALE
    0220-1896Equisetum hyemaleEQUISETUM HYEMALE
    15631-0179EQUISETUM HYEMALEEQUISETUM HYEMALE
    15631-0578EQUISETUM HYEMALEEQUISETUM HYEMALE
    37662-0673Equisetum HyemaleEquisetum Hyemale
    37662-0674Equisetum HyemaleEquisetum Hyemale
    37662-0675Equisetum HyemaleEquisetum Hyemale
    37662-0676Equisetum HyemaleEquisetum Hyemale
    37662-0677Equisetum HyemaleEquisetum Hyemale
    37662-0678Equisetum HyemaleEquisetum Hyemale
    37662-0679Equisetum HyemaleEquisetum Hyemale
    37662-0680Equisetum HyemaleEquisetum Hyemale
    68428-368Equisetum hyemaleEQUISETUM HYEMALE
    71919-269Equisetum hyemaleEQUISETUM HYEMALE
    64117-142IncontinenceEQUISETUM HYEMALE

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