Label: BRYONIA ALBA pellet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

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 August 21, 2012

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  • WARNING

    WARNING: DO NOT USE IF PLASTIC OUTER SEAL AROUND CAP BROKEN OR MISSING.

    IF SYMPTOMS WORSEN OR PERSIST OR IF PREGNANT OR NURSING, SEEK ADVICE OF A DOCTOR

  • Keep out of reach of children

    KEEP ALL MEDICINES OUT OF THE REACH OF CHILDREN.

  • MAXIMUM DOSE

    MAXIMUM DOSE:

    ADULT: 4 pellets, 4 times a day or less.

    CHILDREN: 1/2 of adult dose

  • Active Ingredient

    Bryonia Alba 30C

  • Inactive ingredient

    NON LACTOSE PELLETS:

    70% sucrose, 30% starch of corn.

  • Usage

    USES: PER STANDARD HOMEOPATHIC INDICATIONS.

    Purpose

    USES: PER STANDARD HOMEOPATHIC INDICATIONS.

  • Manufacturer Info, etc.

    CONTAINS NO LACTOSE OR ANIMAL PRODUCTS

    MADE IN THE U.S.A.

    NDC #57471

    1-800-607-7447 KENT and ALLEN MADISON, WI 53714

  • KOSHER

    KOSHER PARVE #1992

  • Traditional Homeopathic Medicine

    TRADITIONAL HOMEOPATHIC MEDICINE (Generation #1)

  • Principal display panel

    BRYONIA ALBA

    30C

    800 PELLETS

    HOM 073

    image of bottle label

  • INGREDIENTS AND APPEARANCE
    BRYONIA ALBA 
    bryonia alba pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57471-3061
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT30 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColorwhiteScore    
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57471-3061-3800 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/01/1988
    Labeler - Celletech Ltd. (781002985)
    Establishment
    NameAddressID/FEIBusiness Operations
    Celletech Ltd.781002985manufacture(57471-3061)
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