NDC 15631-0543

BRYONIA ALBA

Bryonia Alba

BRYONIA ALBA 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 Bryonia Alba Root.

Product ID15631-0543_42218b60-b6eb-4470-ae40-f9cacec74f54
NDC15631-0543
Product TypeHuman Otc Drug
Proprietary NameBRYONIA ALBA
Generic NameBryonia Alba
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
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 15631-0543-3

100 TABLET in 1 CONTAINER (15631-0543-3)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0543-7 [15631054307]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0543-3 [15631054303]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0543-0 [15631054300]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0543-4 [15631054304]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0543-1 [15631054301]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0543-6 [15631054306]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0543-2 [15631054302]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0543-5 [15631054305]

BRYONIA ALBA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BRYONIA ALBA ROOT3 [hp_X]/1

OpenFDA Data

SPL SET ID:3f7638ac-7936-440d-8c24-cf51f54ad653
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.