Bryonia Eucalyptus Flu Relief: Homeopathic Product Information

BRYONIA EUCALYPTUS FLU RELIEF — aconitum napellus root, bryonia cretica subsp. dioica root, eupatorium cannabinum whole flowering, cinchona officinalis bark and eucalyptus globulus leaf pellet
Uriel Pharmacy Inc

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Purpose

Uses: Temporarily relieves symptoms of influenza (flu).

Dosage & Administration

Directions: Dissolve under tongue every hour as needed, decreasing to 4 times daily as symptoms improve. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.

OTC-Active Ingredient

Active Ingredients: Aconitum e tub. 3X, Bryonia e rad. 3X, Eupatorium cann. ex herba 3X, China e cort. 3X, Eucalyptus e fol. 3X, all HPUS.

Inactive Ingredient

Inactive Ingredient: Sucrose, Vivianite 7X.

Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN.

Do not use section

Warnings:Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

Ask doctor section

Consult a doctor if symptoms are serious or persist for 3 days, if you are diabetic or intolerant of sugar.

Pregnancy or breast feeding section

If you are pregnant or nursing, consult a doctor before use.

Questions section

Questions? Uriel Pharmacy

866 642-2858 East Troy, WI 53120

www.urielpharmacy.com

NDC 48951-2084-2

Principal Display Panel

Bryonia Eucalyptus

Flu Relief

Homeopathic Pellets

net wt. 1 oz.

bryonia eucalyptus pellets bottle label
(click image for full-size original)
BRYONIA EUCALYPTUS FLU RELIEF
aconitum napellus root bryonia cretica subsp. dioica root eupatorium cannabinum whole flowering cinchona officinalis bark eucalyptus globulus leaf pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-2084
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACONITUM NAPELLUS ROOT (ACONITUM NAPELLUS ROOT) ACONITUM NAPELLUS ROOT 3 [hp_X]
BRYONIA CRETICA SUBSP. DIOICA ROOT (BRYONIA CRETICA SUBSP. DIOICA ROOT) BRYONIA CRETICA SUBSP. DIOICA ROOT 3 [hp_X]
EUPATORIUM CANNABINUM WHOLE FLOWERING (EUPATORIUM CANNABINUM WHOLE FLOWERING) EUPATORIUM CANNABINUM WHOLE FLOWERING 3 [hp_X]
CINCHONA OFFICINALIS BARK (CINCHONA OFFICINALIS BARK) CINCHONA OFFICINALIS BARK 3 [hp_X]
EUCALYPTUS GLOBULUS LEAF (EUCALYPTUS GLOBULUS LEAF) EUCALYPTUS GLOBULUS LEAF 3 [hp_X]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white (white) Score no score
Shape ROUND (round) Size 3mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:48951-2084-2 1350 PELLET (PELLET) in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 12/01/2009
Labeler — Uriel Pharmacy Inc (043471163)
Establishment
Name Address ID/FEI Operations
Uriel Pharmacy Inc 043471163 manufacture

Revised: 12/2009 Uriel Pharmacy Inc

HomeoLabels.com provides trustworthy package insert and label information about marketed homeopathic remedies as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by HomeoLabels.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

Main Sections

Homeopathy Information by RSS

We source our database directly from the FDA's central repository of homeopathic remedy labels and package inserts, under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.