NDC 15631-0398

SENECIO AUREUS

Senecio Aureus

SENECIO AUREUS 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 Packera Aurea.

Product ID15631-0398_8fd5326d-71ec-49d8-b2eb-6b14fbbc7d5a
NDC15631-0398
Product TypeHuman Otc Drug
Proprietary NameSENECIO AUREUS
Generic NameSenecio Aureus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePACKERA AUREA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0398-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0398-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0398-2 [15631039802]

SENECIO AUREUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0398-5 [15631039805]

SENECIO AUREUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0398-4 [15631039804]

SENECIO AUREUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0398-1 [15631039801]

SENECIO AUREUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0398-0 [15631039800]

SENECIO AUREUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0398-3 [15631039803]

SENECIO AUREUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
PACKERA AUREA1 [hp_X]/1

OpenFDA Data

SPL SET ID:f11332a9-dd7e-4f10-911b-c85c9f23561c
Manufacturer
UNII

NDC Crossover Matching brand name "SENECIO AUREUS" or generic name "Senecio Aureus"

NDCBrand NameGeneric Name
0220-4630Senecio aureusPACKERA AUREA
15631-0398SENECIO AUREUSSENECIO AUREUS
68428-632Senecio aureusPACKERA AUREA
71919-623Senecio aureusPACKERA AUREA

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