NDC 15631-0355

POLYPORUS PINICOLA

Polyporus Pinicola

POLYPORUS PINICOLA 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 Fomitopsis Pinicola Fruiting Body.

Product ID15631-0355_688a7305-2f0b-4a45-8d46-3cc232e3062f
NDC15631-0355
Product TypeHuman Otc Drug
Proprietary NamePOLYPORUS PINICOLA
Generic NamePolyporus Pinicola
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFOMITOPSIS PINICOLA FRUITING BODY
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0355-0

100 PELLET in 1 PACKAGE (15631-0355-0)
Marketing Start Date2015-09-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0355-2 [15631035502]

POLYPORUS PINICOLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-12
Inactivation Date2020-01-31

NDC 15631-0355-1 [15631035501]

POLYPORUS PINICOLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-12
Inactivation Date2020-01-31

NDC 15631-0355-3 [15631035503]

POLYPORUS PINICOLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-12
Inactivation Date2020-01-31

NDC 15631-0355-4 [15631035504]

POLYPORUS PINICOLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-12
Inactivation Date2020-01-31

NDC 15631-0355-5 [15631035505]

POLYPORUS PINICOLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-12
Inactivation Date2020-01-31

NDC 15631-0355-0 [15631035500]

POLYPORUS PINICOLA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-12
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FOMITOPSIS PINICOLA FRUITING BODY2 [hp_X]/1

OpenFDA Data

SPL SET ID:9e2d6f49-d421-41a9-9498-04c28c2a8113
Manufacturer
UNII

NDC Crossover Matching brand name "POLYPORUS PINICOLA" or generic name "Polyporus Pinicola"

NDCBrand NameGeneric Name
15631-0355POLYPORUS PINICOLAPOLYPORUS PINICOLA
71919-553Polyporus pinicolaFOMITOPSIS PINICOLA FRUITING BODY

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