NDC 15631-0356

POTHOS FOETIDUS

Pothos Foetidus

POTHOS FOETIDUS 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 Symplocarpus Foetidus Root.

Product ID15631-0356_140ee4a6-5373-47e2-a1e8-2f3ed54bb3fb
NDC15631-0356
Product TypeHuman Otc Drug
Proprietary NamePOTHOS FOETIDUS
Generic NamePothos Foetidus
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 NameSYMPLOCARPUS FOETIDUS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0356-5

12500 PELLET in 1 PACKAGE (15631-0356-5)
Marketing Start Date2015-09-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0356-0 [15631035600]

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

NDC 15631-0356-1 [15631035601]

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

NDC 15631-0356-3 [15631035603]

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

NDC 15631-0356-2 [15631035602]

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

NDC 15631-0356-5 [15631035605]

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

NDC 15631-0356-4 [15631035604]

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

Drug Details

Active Ingredients

IngredientStrength
SYMPLOCARPUS FOETIDUS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:1fe6bac9-2d00-4976-8f5d-735fb37324af
Manufacturer
UNII

NDC Crossover Matching brand name "POTHOS FOETIDUS" or generic name "Pothos Foetidus"

NDCBrand NameGeneric Name
15631-0356POTHOS FOETIDUSPOTHOS FOETIDUS
15631-0660POTHOS FOETIDUSPOTHOS FOETIDUS

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