Label: BACH ORIGINAL FLOWER REMEDIES HONEYSUCKLE- lonicera caprifolium solution

  • NDC Code(s): 57687-215-10
  • 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 September 29, 2022

If you are a consumer or patient please visit this version.

  • Active ingredient

    Honeysuckle (Lonicera caprifolium) 5X HPUS

    ‘HPUS’ indicates the ingredient is in the official Homeopathic Pharmacopoeia of the United States

  • Purpose

    Embrace the now

  • Use

    For relief of naturally occurring simple nervous tension

  • Warnings

    Consult a doctor if symptoms last for more than 7 days or worsen.

    Keep out of reach of children.

    If pregnant or breast-feeding, ask a health professional before use.

  • Directions

    Take 2 drops directly on the tongue or add to a beverage & sip. Repeat as needed throughout the day.

    Children under 2: ask a doctor before use.

  • Other information

    Store below 77 ºF (25 ºC)

    Do not use if tamper evident seal around bottle neck is missing or broken

  • Inactive ingredients

    glycerin [vegetable], purified water

  • Questions

    800-319-9151 8am-5pm (EST) Mon-Fri

  • PRINCIPAL DISPLAY PANEL

    Bach Original Flower Remedies Honeysuckle

  • INGREDIENTS AND APPEARANCE
    BACH ORIGINAL FLOWER REMEDIES HONEYSUCKLE 
    lonicera caprifolium solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57687-215
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY) (LONICERA CAPRIFOLIUM FLOWERING TOP - UNII:1X0T378SXY) LONICERA CAPRIFOLIUM FLOWERING TOP5 [hp_X]  in 0.095 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57687-215-101 in 1 CARTON09/20/2022
    110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/20/2022
    Labeler - Nelson Bach USA Limited (877720193)
    Registrant - A. Nelson & Co. Limited (221471234)
    Establishment
    NameAddressID/FEIBusiness Operations
    A. Nelson & Co. Limited221471234manufacture(57687-215)