NDC 15631-0465

XANTHOXYLUM FRAXINEUM

Xanthoxylum Fraxineum

XANTHOXYLUM FRAXINEUM 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 Zanthoxylum Americanum Bark.

Product ID15631-0465_26624913-a819-4886-9bcc-f7230457915c
NDC15631-0465
Product TypeHuman Otc Drug
Proprietary NameXANTHOXYLUM FRAXINEUM
Generic NameXanthoxylum Fraxineum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameZANTHOXYLUM AMERICANUM BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0465-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0465-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0465-2 [15631046502]

XANTHOXYLUM FRAXINEUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0465-4 [15631046504]

XANTHOXYLUM FRAXINEUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0465-0 [15631046500]

XANTHOXYLUM FRAXINEUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0465-1 [15631046501]

XANTHOXYLUM FRAXINEUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0465-3 [15631046503]

XANTHOXYLUM FRAXINEUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0465-5 [15631046505]

XANTHOXYLUM FRAXINEUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
ZANTHOXYLUM AMERICANUM BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:f624e19e-4e0c-4b97-8776-b17fec8c40b5
Manufacturer
UNII

NDC Crossover Matching brand name "XANTHOXYLUM FRAXINEUM" or generic name "Xanthoxylum Fraxineum"

NDCBrand NameGeneric Name
0220-5335Xanthoxylum fraxineumZANTHOXYLUM AMERICANUM BARK
15631-0465XANTHOXYLUM FRAXINEUMXANTHOXYLUM FRAXINEUM
68428-709Xanthoxylum fraxineumZANTHOXYLUM AMERICANUM BARK
71919-720XANTHOXYLUM FRAXINEUMZanthoxylum americanum

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