Label: BAURI 40 (NUMBER 22)- lycopodium, 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 February 5, 2018

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

  • DRUG FACTS: Active Ingredients

    Bryonia alba 30C HPUS, Lycopodium clavatum 30C HPUS

  • Inactive Ingredients

    Sucrose, Lactose

  • Purpose

    Relieves burning and irritation during urination

  • Uses

    Relieves burning and irritation during urination

  • 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: Take three pills daily. Leaving a gap of 30 minutes after 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

    Bauri 40

    NDC: 69152-0022-1

    Bauri 40

    Number 22

    Homeopathic Medicine

    Relieves burning and irritation during urination

    96 Pills (Approx.)

    Product of USA

  • INGREDIENTS AND APPEARANCE
    BAURI 40 (NUMBER 22) 
    lycopodium, bryonia alba pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69152-0022
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE30 [hp_C]
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT30 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    ColorwhiteScore    
    ShapeROUNDSize4mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69152-0022-196 in 1 BOTTLE; Type 0: Not a Combination Product02/05/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/26/2014
    Labeler - Paramesh Banerji Life Sciences LLC (079393726)
    Establishment
    NameAddressID/FEIBusiness Operations
    Paramesh Banerji Life Sciences LLC079393726manufacture(69152-0022) , pack(69152-0022) , label(69152-0022)