Label: HYPERICUM PERFORATUM 200C- hypericum perforatum 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 April 28, 2016

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  • DRUG FACTS: Active Ingredient

    Hypericum perforatum 200C HPUS

  • Inactive Ingredients

    Sucrose, Lactose

  • Purpose

    Neuralgic pain and sprains

  • Uses

    Neuralgic pain and sprains

  • 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

    Hypericum perforatum 200C

    NDC: 69152-1009-1

    Hypericum perforatum 200C

    Homeopathic Medicine

    Neuralgic pain and sprains

    96 Pills (Approx.)

    Product of USA

  • INGREDIENTS AND APPEARANCE
    HYPERICUM PERFORATUM 200C 
    hypericum perforatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69152-1009
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM200 [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:69152-1009-196 in 1 BOTTLE; Type 0: Not a Combination Product05/12/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/12/2015
    Labeler - Paramesh Banerji Life Sciences LLC (079393726)
    Establishment
    NameAddressID/FEIBusiness Operations
    Paramesh Banerji Life Sciences LLC079393726manufacture(69152-1009) , pack(69152-1009) , label(69152-1009)
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