NDC 15631-0660

POTHOS FOETIDUS

Pothos Foetidus

POTHOS FOETIDUS 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 Symplocarpus Foetidus Root.

Product ID15631-0660_95b3f428-70ee-47bd-a74a-70d11b034507
NDC15631-0660
Product TypeHuman Otc Drug
Proprietary NamePOTHOS FOETIDUS
Generic NamePothos Foetidus
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 NameSYMPLOCARPUS FOETIDUS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0660-5

500 TABLET in 1 CONTAINER (15631-0660-5)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0660-4 [15631066004]

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

NDC 15631-0660-7 [15631066007]

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

NDC 15631-0660-0 [15631066000]

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

NDC 15631-0660-2 [15631066002]

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

NDC 15631-0660-5 [15631066005]

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

NDC 15631-0660-6 [15631066006]

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

NDC 15631-0660-1 [15631066001]

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

NDC 15631-0660-3 [15631066003]

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

Drug Details

Active Ingredients

IngredientStrength
SYMPLOCARPUS FOETIDUS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:7935b337-e6c0-4b48-834d-12b1f533adab
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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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