NDC 48951-2084

Bryonia Eucalyptus Flu Relief

Aconitum Napellus Root Bryonia Cretica Subsp. Dioica Root Eupatorium Cannabinum Whole Flowering Cinchona Officinalis Bark Eucalyptus Globulus Leaf

Bryonia Eucalyptus Flu Relief is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc. The primary component is Aconitum Napellus Root; Bryonia Cretica Subsp. Dioica Root; Eupatorium Cannabinum Whole Flowering; Cinchona Officinalis Bark; Eucalyptus Globulus Leaf.

Product ID48951-2084_12742f30-e03b-11de-8a39-0800200c9a66
NDC48951-2084
Product TypeHuman Otc Drug
Proprietary NameBryonia Eucalyptus Flu Relief
Generic NameAconitum Napellus Root Bryonia Cretica Subsp. Dioica Root Eupatorium Cannabinum Whole Flowering Cinchona Officinalis Bark Eucalyptus Globulus Leaf
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2009-12-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc
Substance NameACONITUM NAPELLUS ROOT; BRYONIA CRETICA SUBSP. DIOICA ROOT; EUPATORIUM CANNABINUM WHOLE FLOWERING; CINCHONA OFFICINALIS BARK; EUCALYPTUS GLOBULUS LEAF
Active Ingredient Strength3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 48951-2084-2

1350 PELLET in 1 BOTTLE, GLASS (48951-2084-2)
Marketing Start Date2009-12-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-2084-2 [48951208402]

Bryonia Eucalyptus Flu Relief PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACONITUM NAPELLUS ROOT3 [hp_X]/1

OpenFDA Data

SPL SET ID:9a61ae10-e04d-11de-8a39-0800200c9a66
Manufacturer
UNII

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