Label: CHELIDONIUM MAJUS 6X- chelidonium majus liquid

  • 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 March 10, 2017

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

  • DRUG FACTS: Active Ingredient

    Chelidonium majus 6X HPUS

  • Inactive Ingredient

    Ethyl alcohol

  • Purpose

    Chest congestion & related fever

  • Uses

    Chest congestion & related fever

  • Warnings

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

  • Keep out of reach of children

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Direction

    Adult or child: Five drops in 3 tea spoons of water, leaving a gap of 30 minutes from any food or as advised by your physician.

  • Manufactured by

    Paramesh Banerji Life Sciences, LLC.

    North Brunswick, NJ 08902, USA.

    Tel: +1-732-743-5936

    Email: info@pblifesciences.com

  • Principal Display Panel

    Chelidonium majus 6X

    NDC: 69152-1214-1

    Chelidonium majus 6X

    Homeopathic Medicine

    Liquid

    Chest congestion & related fever

    8 mL (Approx.)

    Product of USA

  • INGREDIENTS AND APPEARANCE
    CHELIDONIUM MAJUS 6X 
    chelidonium majus liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69152-1214
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS6 [hp_X]  in 8 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69152-1214-18 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/25/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/25/2015
    Labeler - Paramesh Banerji Life Sciences LLC (079393726)
    Establishment
    NameAddressID/FEIBusiness Operations
    Paramesh Banerji Life Sciences LLC079393726pack(69152-1214) , manufacture(69152-1214) , label(69152-1214)