RUTA GRAVEOLENS 200C (RUTA GRAVEOLENS) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]

RUTA GRAVEOLENS 200C (RUTA GRAVEOLENS) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]
PDF | XML

NDC 69152-1098-1
Set ID 18254f17-f2d2-212e-e054-00144ff8d46c
Category HUMAN OTC DRUG LABEL
Packager Paramesh Banerji Life Sciences LLC
Generic Name
Product Class
Product Number
Application Number
  • DRUG FACTS: Active Ingredient

    Ruta graveolens 200C HPUS

  • Inactive Ingredients

    Sucrose, Lactose

  • Purpose

    Bony growths

  • Uses

    Bony growths

  • 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

    www.pblifesciences.com/permapotent

  • Principal Display Panel

    Ruta graveolens 200C

    NDC: 69152-1098-1

    Ruta graveolens 200C

    Homeopathic Medicine

    Bony growths

    96 Pills (Approx.)

    Product of USA

  • INGREDIENTS AND APPEARANCE
    RUTA GRAVEOLENS 200C 
    ruta graveolens pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69152-1098
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP200 [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:69152-1098-196 in 1 BOTTLE; Type 0: Not a Combination Product06/10/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/10/2015
    Labeler - Paramesh Banerji Life Sciences LLC (079393726)
    Establishment
    NameAddressID/FEIBusiness Operations
    Paramesh Banerji Life Sciences LLC079393726pack(69152-1098) , label(69152-1098) , manufacture(69152-1098)

Related Drugs