Label: BRYONIA EUCALYPTUS FLU RELIEF- aconitum napellus root bryonia cretica subsp. dioica root eupatorium cannabinum whole flowering cinchona officinalis bark eucalyptus globulus leaf pellet

  • Category: HUMAN OTC DRUG LABEL

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.

Drug Label Information

Updated December 3, 2009

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  • 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

  • INGREDIENTS AND APPEARANCE
    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 TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2084
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACONITUM NAPELLUS ROOT (UNII: KPD2N7348X) (ACONITUM NAPELLUS ROOT - UNII:KPD2N7348X) ACONITUM NAPELLUS ROOT3 [hp_X]
    BRYONIA CRETICA SUBSP. DIOICA ROOT (UNII: 53UB5FH7CX) (BRYONIA CRETICA SUBSP. DIOICA ROOT - UNII:53UB5FH7CX) BRYONIA CRETICA SUBSP. DIOICA ROOT3 [hp_X]
    EUPATORIUM CANNABINUM WHOLE FLOWERING (UNII: A5296YC7FS) (EUPATORIUM CANNABINUM WHOLE FLOWERING - UNII:A5296YC7FS) EUPATORIUM CANNABINUM WHOLE FLOWERING3 [hp_X]
    CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK3 [hp_X]
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF3 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Colorwhite (white) Scoreno score
    ShapeROUND (round) Size3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-2084-21350 in 1 BOTTLE, GLASS
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/01/2009
    Labeler - Uriel Pharmacy Inc (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc043471163manufacture
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