NDC 15631-0199

FUCUS VESICULOSUS

Fucus Vesiculosus

FUCUS VESICULOSUS 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 Fucus Vesiculosus.

Product ID15631-0199_94a0fb24-193e-4ce6-8c5b-f5c2f07d9524
NDC15631-0199
Product TypeHuman Otc Drug
Proprietary NameFUCUS VESICULOSUS
Generic NameFucus Vesiculosus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-25
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 15631-0199-0

100 PELLET in 1 PACKAGE (15631-0199-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0199-0 [15631019900]

FUCUS VESICULOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0199-2 [15631019902]

FUCUS VESICULOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0199-5 [15631019905]

FUCUS VESICULOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0199-3 [15631019903]

FUCUS VESICULOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0199-4 [15631019904]

FUCUS VESICULOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0199-1 [15631019901]

FUCUS VESICULOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
FUCUS VESICULOSUS1 [hp_X]/1

OpenFDA Data

SPL SET ID:a96bf58d-660d-4908-8ab4-b8c206b54cf1
Manufacturer
UNII

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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