NDC 15631-0587

FUCUS VESICULOSUS

Fucus Vesiculosus

FUCUS VESICULOSUS 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 Fucus Vesiculosus.

Product ID15631-0587_849f370f-27e6-4ee8-a8fc-5a665372a8df
NDC15631-0587
Product TypeHuman Otc Drug
Proprietary NameFUCUS VESICULOSUS
Generic NameFucus Vesiculosus
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-01-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFUCUS VESICULOSUS
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0587-5

500 TABLET in 1 CONTAINER (15631-0587-5)
Marketing Start Date2016-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0587-3 [15631058703]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0587-2 [15631058702]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0587-4 [15631058704]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0587-0 [15631058700]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0587-6 [15631058706]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0587-5 [15631058705]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0587-7 [15631058707]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0587-1 [15631058701]

FUCUS VESICULOSUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FUCUS VESICULOSUS1 [hp_X]/1

OpenFDA Data

SPL SET ID:1c01957b-12d2-4eff-bc34-f5b7a67515b2
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "FUCUS VESICULOSUS" or generic name "Fucus Vesiculosus"

    NDCBrand NameGeneric Name
    0220-2165Fucus vesiculosusFUCUS VESICULOSUS
    0220-2167Fucus vesiculosusFUCUS VESICULOSUS
    15631-0199FUCUS VESICULOSUSFUCUS VESICULOSUS
    15631-0587FUCUS VESICULOSUSFUCUS VESICULOSUS
    57520-0676Fucus VesiculosusFucus vesiculosus,
    60512-6695FUCUS VESICULOSUSFUCUS VESICULOSUS
    68428-944Fucus vesiculosusFUCUS VESICULOSUS
    71919-304Fucus vesiculosusFUCUS VESICULOSUS
    58264-0106D-100Fucus vesiculosus

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