Label: EUPATORIUM PERFOLIATUM pellet

  • NDC Code(s): 37662-0996-1, 37662-0996-2, 37662-0996-3, 37662-0997-1, view more
    37662-0997-2, 37662-0997-3, 37662-0998-1, 37662-0998-2, 37662-0998-3, 37662-0998-4, 37662-0999-1, 37662-0999-2, 37662-0999-3, 37662-0999-4, 37662-1000-1, 37662-1000-2, 37662-1000-3, 37662-1000-4, 37662-1001-1, 37662-1001-2, 37662-1001-3, 37662-1001-4, 37662-1002-1, 37662-1002-2, 37662-1002-3, 37662-1002-4, 37662-1003-1, 37662-1003-2, 37662-1003-3, 37662-1003-4, 37662-1004-1
  • Packager: Hahnemann Laboratories, INC.
  • 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 July 20, 2022

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

  • ACTIVE INGREDIENT

  • DOSAGE FORMS & STRENGTHS

  • ACTIVE INGREDIENT

  • PURPOSE

  • INDICATIONS & USAGE

  • WARNINGS

  • PREGNANCY OR BREAST FEEDING

  • ASK DOCTOR

  • KEEP OUT OF REACH OF CHILDREN

  • INSTRUCTIONS FOR USE

  • DOSAGE & ADMINISTRATION

  • ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION

  • INACTIVE INGREDIENT

  • QUESTIONS

  • PRINCIPAL DISPLAY PANEL

    Eupatorium Perfoliatum 6C 5gEupatorium Perfoliatum 6C 30gEupatorium Perfoliatum 6C 100gEupatorium Perfoliatum 12C 5gEupatorium Perfoliatum 12C 30gEupatorium Perfoliatum 12C 100gEupatorium Perfoliatum 30C 1gEupatorium Perfoliatum 30C 5gEupatorium Perfoliatum 30C 30gEupatorium Perfoliatum 30C 100gEupatorium Perfoliatum 100C 1gEupatorium Perfoliatum 100C 5gEupatorium Perfoliatum 100C 30gEupatorium Perfoliatum 100C 100gEupatorium Perfoliatum 200C 1gEupatorium Perfoliatum 200C 5gEupatorium Perfoliatum 200C 30gEupatorium Perfoliatum 200C 100gEupatorium Perfoliatum 500C 1gEupatorium Perfoliatum 500C 5gEupatorium Perfoliatum 500C 30gEupatorium Perfoliatum 500C 100gEupatorium Perfoliatum 1M 1gEupatorium Perfoliatum 1M 5gEupatorium Perfoliatum 1M 30gEupatorium Perfoliatum 1M 100gEupatorium Perfoliatum 10M 1gEupatorium Perfoliatum 10M 5gEupatorium Perfoliatum 10M 30gEupatorium Perfoliatum 10M 100gEupatorium Perfoliatum LM1 30g

  • INGREDIENTS AND APPEARANCE
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0996
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA6 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0996-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-0996-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-0996-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA1 [hp_M]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-1002-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-1002-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-1002-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    4NDC:37662-1002-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1004
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA1 [hp_Q]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize1mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-1004-110000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1003
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA10 [hp_M]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-1003-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-1003-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-1003-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    4NDC:37662-1003-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA500 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-1001-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-1001-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-1001-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    4NDC:37662-1001-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0997
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA12 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0997-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-0997-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-0997-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0998
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA30 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0998-180 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-0998-2200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-0998-31200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    4NDC:37662-0998-44000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0999
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA100 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0999-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-0999-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-0999-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    4NDC:37662-0999-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    EUPATORIUM PERFOLIATUM 
    eupatorium perfoliatum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1000
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIANELLA QUINQUEFOLIA (UNII: 50L35LKK9W) (GENTIANELLA QUINQUEFOLIA - UNII:50L35LKK9W) GENTIANELLA QUINQUEFOLIA200 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-1000-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    2NDC:37662-1000-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/20/2022
    3NDC:37662-1000-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    4NDC:37662-1000-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2022
    Labeler - Hahnemann Laboratories, INC. (147098081)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hahnemann Laboratories, INC.147098081manufacture(37662-0996, 37662-0997, 37662-0998, 37662-0999, 37662-1000, 37662-1001, 37662-1002, 37662-1003, 37662-1004)