Label: BACH ORIGINAL FLOWER REMEDIES- agrimonia eupatoria solution

  • NDC Code(s): 57687-250-20
  • Packager: Nelson Bach USA Limited
  • 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 May 14, 2020

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  • Indication

    For relief of naturally occurring simple nervous tension.

  • Directions

    Take 2 drops in mouth or in water, sip at intervals. Repeat as needed.

  • Active Ingredient

    5X dilution of Agrimony (Agrimonia eupatoria) HPUS.

  • Inactive Ingredient

    27% Alcohol.

  • Warnings

    Keep out of reach of children.

    If pregnant or breastfeeding, ask a health professional before use.

  • Other Information

    Do not use if seal is broken. Store below 25°C / 77℉. Satisfaction Guaranteed.

  • QUESTIONS

    If unsatisfied call 1-800-319-9151 for refund. BachRemedies.com

  • SPL UNCLASSIFIED SECTION

    Distributed by
    Nelson Bach USA Ltd.
    21 High St., Suite 302
    North Andover, MA
    01845

  • PRINCIPAL DISPLAY PANEL - 20 mL Bottle Label

    Bach®
    ORIGINAL
    FLOWER REMEDIES

    AGRIMONY

    Communicate Openly*

    20 mL (0.7 fl oz)
    HOMEOPATHIC
    CONTAINS 27% ALCOHOL

    PRINCIPAL DISPLAY PANEL - 20 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    BACH ORIGINAL FLOWER REMEDIES 
    agrimonia eupatoria solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57687-250
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Agrimonia eupatoria (UNII: EBU0U94820) (Agrimonia eupatoria - UNII:EBU0U94820) Agrimonia eupatoria5 [hp_X]  in 0.095 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57687-250-2020 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/01/2002
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED HOMEOPATHIC01/01/2002
    Labeler - Nelson Bach USA Limited (877720193)
    Registrant - A. Nelson & Co. Limited (221471234)
    Establishment
    NameAddressID/FEIBusiness Operations
    A. Nelson & Co Ltd221471234MANUFACTURE(57687-250, 57687-250) , PACK(57687-250) , LABEL(57687-250)
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