FOENICULUM VULGARE- foeniculum vulgare pellet 
Hahnemann Laboratories, INC.

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.

----------

Gratiola Officinalis 6C 5gGratiola Officinalis 6C 30gGratiola Officinalis 6C 100gGratiola Officinalis 12C 5gGratiola Officinalis 12C 30gGratiola Officinalis 12C 100gGratiola Officinalis 30C 1gGratiola Officinalis 30C 5gGratiola Officinalis 30C 30gGratiola Officinalis 30C 100gGratiola Officinalis 100C 1gGratiola Officinalis 100C 5gGratiola Officinalis 100C 30gGratiola Officinalis 100C 100gGratiola Officinalis 200C 1gGratiola Officinalis 200C 5gGratiola Officinalis 200C 30gGratiola Officinalis 200C 100gGratiola Officinalis 500C 1gGratiola Officinalis 500C 5gGratiola Officinalis 500C 30gGratiola Officinalis 500C 100gGratiola Officinalis 1M 1gGratiola Officinalis 1M 5gGratiola Officinalis 1M 30gGratiola Officinalis 1M 100g

FOENICULUM VULGARE 
foeniculum vulgare pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0746
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRATIOLA OFFICINALIS (UNII: BDD9991A36) (GRATIOLA OFFICINALIS - UNII:BDD9991A36) GRATIOLA OFFICINALIS500 [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:37662-0746-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0746-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0746-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0746-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
FOENICULUM VULGARE 
foeniculum vulgare pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0747
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRATIOLA OFFICINALIS (UNII: BDD9991A36) (GRATIOLA OFFICINALIS - UNII:BDD9991A36) GRATIOLA OFFICINALIS1 [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:37662-0747-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0747-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0747-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0747-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
FOENICULUM VULGARE 
foeniculum vulgare pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0741
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRATIOLA OFFICINALIS (UNII: BDD9991A36) (GRATIOLA OFFICINALIS - UNII:BDD9991A36) GRATIOLA OFFICINALIS6 [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:37662-0741-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0741-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0741-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
FOENICULUM VULGARE 
foeniculum vulgare pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0743
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRATIOLA OFFICINALIS (UNII: BDD9991A36) (GRATIOLA OFFICINALIS - UNII:BDD9991A36) GRATIOLA OFFICINALIS30 [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:37662-0743-180 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0743-2200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0743-31200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0743-44000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
FOENICULUM VULGARE 
foeniculum vulgare pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0745
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRATIOLA OFFICINALIS (UNII: BDD9991A36) (GRATIOLA OFFICINALIS - UNII:BDD9991A36) GRATIOLA OFFICINALIS200 [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:37662-0745-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0745-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0745-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0745-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
FOENICULUM VULGARE 
foeniculum vulgare pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0742
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRATIOLA OFFICINALIS (UNII: BDD9991A36) (GRATIOLA OFFICINALIS - UNII:BDD9991A36) GRATIOLA OFFICINALIS12 [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:37662-0742-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0742-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0742-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
FOENICULUM VULGARE 
foeniculum vulgare pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0744
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRATIOLA OFFICINALIS (UNII: BDD9991A36) (GRATIOLA OFFICINALIS - UNII:BDD9991A36) GRATIOLA OFFICINALIS100 [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:37662-0744-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0744-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0744-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0744-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
Labeler - Hahnemann Laboratories, INC. (147098081)
Establishment
NameAddressID/FEIBusiness Operations
Hahnemann Laboratories, INC.147098081manufacture(37662-0741, 37662-0742, 37662-0743, 37662-0744, 37662-0745, 37662-0746, 37662-0747)

Revised: 7/2022
Document Id: e32c56fe-69d6-23c7-e053-2a95a90a51bd
Set id: e32c56fe-69d5-23c7-e053-2a95a90a51bd
Version: 1
Effective Time: 20220706
 
Hahnemann Laboratories, INC.