Label: MEDORRHINUM- gonorrheal urethral secretion human pellet

  • Category: HUMAN PRESCRIPTION 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 December 21, 2023

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

  • Active Ingredients

    Medorrhinum 12X

  • PURPOSE

  • Use

    Rx only*

  • Warnings

    Stop use and ask a doctor if

    symptoms persist for more than 3 days or worsen.

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

  • Directions

    5 pellets 3 times a day until symptoms are relieved.

  • Other information

    Do not use if pellet dispenser seal is broken.
    contains approx. 80 pellets

  • Inactive ingredients

    lactose, sucrose

  • Questions, Comments?

    1-800-BOIRON-1
    Newtown Square, PA 19073-3267
    info@boironusa.com

  • *

    These "Uses" have not been evaluated by the FDA.

  • Principle Display Panel - Medorrhinum HPUS 12X

    12Xlabelimage

  • INGREDIENTS AND APPEARANCE
    MEDORRHINUM 
    gonorrheal urethral secretion human pellet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0220-7309
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (GONORRHEAL URETHRAL SECRETION HUMAN - UNII:9BZG9E3I8F) GONORRHEAL URETHRAL SECRETION HUMAN12 [hp_X]
    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:0220-7309-4180 in 1 TUBE; Type 0: Not a Combination Product03/03/1983
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/03/1983
    Labeler - Laboratoires Boiron (282560473)
    Registrant - Boiron Inc. (014892269)
    Establishment
    NameAddressID/FEIBusiness Operations
    Boiron282560473manufacture(0220-7309)