NDC 15631-0087

BRYONIA ALBA

Bryonia Alba

BRYONIA ALBA 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 Bryonia Alba Root.

Product ID15631-0087_0162c28c-60d5-44ba-9deb-472def251da8
NDC15631-0087
Product TypeHuman Otc Drug
Proprietary NameBRYONIA ALBA
Generic NameBryonia Alba
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 NameBRYONIA ALBA ROOT
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0087-0

100 PELLET in 1 PACKAGE (15631-0087-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0087-5 [15631008705]

BRYONIA ALBA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0087-0 [15631008700]

BRYONIA ALBA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0087-3 [15631008703]

BRYONIA ALBA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0087-4 [15631008704]

BRYONIA ALBA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0087-1 [15631008701]

BRYONIA ALBA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0087-2 [15631008702]

BRYONIA ALBA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

Drug Details

Active Ingredients

IngredientStrength
BRYONIA ALBA ROOT3 [hp_X]/1

OpenFDA Data

SPL SET ID:134c943f-a71d-4321-8201-cb2695374cb8
Manufacturer
UNII

NDC Crossover Matching brand name "BRYONIA ALBA" or generic name "Bryonia Alba"

NDCBrand NameGeneric Name
15631-0087BRYONIA ALBABRYONIA ALBA
15631-0543BRYONIA ALBABRYONIA ALBA
53645-1880Bryonia AlbaBryonia Alba
54973-0607BRYONIA ALBAbryonia alba root
54973-2907BRYONIA ALBAbryonia alba root
57471-3061Bryonia AlbaBryonia Alba
60512-1007BRYONIA ALBABRYONIA ALBA
62106-7530BRYONIA ALBAWhite bryony
63545-548Bryonia AlbaBryonia Alba
63545-549Bryonia AlbaBryonia Alba
63545-551Bryonia AlbaBryonia Alba
63545-552Bryonia AlbaBryonia Alba
63545-553Bryonia AlbaBryonia Alba
63545-554Bryonia AlbaBryonia Alba
63545-555Bryonia AlbaBryonia Alba
63545-556Bryonia AlbaBryonia Alba
63545-557Bryonia AlbaBryonia Alba
66096-802Bryonia AlbaBRYONIA ALBA
68428-265Bryonia albaBRYONIA ALBA ROOT
71919-132Bryonia albaBRYONIA ALBA ROOT
76472-3007Bryonia AlbaBRYONIA ALBA ROOT
79718-1024Bryonia AlbaBryonia Alba
79718-1082Bryonia AlbaBryonia Alba
69152-1021Bryonia alba 200CBryonia alba
69152-1014Bryonia alba 30CBryonia alba

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