KALI CHLORICUM- kali chloricum 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.

----------

Kali Chloricum 6C 5gKali Chloricum 6C 30gKali Chloricum 6C 100gKali Chloricum 12C 5gKali Chloricum 12C 30gKali Chloricum 12C 100gKali Chloricum 30C 1gKali Chloricum 30C 5gKali Chloricum 30C 30gKali Chloricum 30C 100gKali Chloricum 100C 1gKali Chloricum 100C 5gKali Chloricum 100C 30gKali Chloricum 100C 100gKali Chloricum 200C 1gKali Chloricum 200C 5gKali Chloricum 200C 30gKali Chloricum 200C 100gKali Chloricum 500C 1gKali Chloricum 500C 5gKali Chloricum 500C 30gKali Chloricum 500C 100gKali Chloricum 1M 1gKali Chloricum 1M 5gKali Chloricum 1M 30gKali Chloricum 1M 100gKali Chloricum LM1 30g

KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0877
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE30 [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:37662-0877-180 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
2NDC:37662-0877-31200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
3NDC:37662-0877-44000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
4NDC:37662-0877-2200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0881
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE1 [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:37662-0881-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
2NDC:37662-0881-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
3NDC:37662-0881-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
4NDC:37662-0881-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0880
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE500 [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:37662-0880-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
2NDC:37662-0880-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
3NDC:37662-0880-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
4NDC:37662-0880-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0882
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE1 [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:37662-0882-110000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0875
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE6 [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:37662-0875-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
2NDC:37662-0875-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
3NDC:37662-0875-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0876
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE12 [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:37662-0876-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
2NDC:37662-0876-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
3NDC:37662-0876-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0878
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE100 [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:37662-0878-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
2NDC:37662-0878-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
3NDC:37662-0878-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
4NDC:37662-0878-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
KALI CHLORICUM 
kali chloricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0879
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE200 [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:37662-0879-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
2NDC:37662-0879-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
3NDC:37662-0879-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/13/2022
4NDC:37662-0879-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/13/2022
Labeler - Hahnemann Laboratories, INC. (147098081)
Establishment
NameAddressID/FEIBusiness Operations
Hahnemann Laboratories, INC.147098081manufacture(37662-0875, 37662-0876, 37662-0877, 37662-0878, 37662-0879, 37662-0880, 37662-0881, 37662-0882)

Revised: 7/2022
Document Id: e3baf111-d3e8-7f7f-e053-2995a90a84e6
Set id: e3baf111-d3e7-7f7f-e053-2995a90a84e6
Version: 1
Effective Time: 20220713
 
Hahnemann Laboratories, INC.