NATRUM SULPHURATUM- natrum sulphuratum 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.

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NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1183
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE1 [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:37662-1183-110000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1177
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE12 [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:37662-1177-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
2NDC:37662-1177-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
3NDC:37662-1177-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1182
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE1 [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:37662-1182-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
2NDC:37662-1182-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
3NDC:37662-1182-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
4NDC:37662-1182-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1176
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE6 [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:37662-1176-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
2NDC:37662-1176-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
3NDC:37662-1176-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1178
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE30 [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:37662-1178-180 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
2NDC:37662-1178-2200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
3NDC:37662-1178-31200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
4NDC:37662-1178-44000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1179
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE100 [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:37662-1179-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
2NDC:37662-1179-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
3NDC:37662-1179-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
4NDC:37662-1179-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1181
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE500 [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:37662-1181-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
2NDC:37662-1181-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
3NDC:37662-1181-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
4NDC:37662-1181-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
NATRUM SULPHURATUM 
natrum sulphuratum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1180
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE200 [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:37662-1180-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
2NDC:37662-1180-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/03/2022
3NDC:37662-1180-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
4NDC:37662-1180-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/03/2022
Labeler - Hahnemann Laboratories, INC. (147098081)
Establishment
NameAddressID/FEIBusiness Operations
Hahnemann Laboratories, INC.147098081manufacture(37662-1176, 37662-1177, 37662-1178, 37662-1179, 37662-1180, 37662-1181, 37662-1182, 37662-1183)

Revised: 8/2022
Document Id: e55f6111-c940-26d0-e053-2995a90ae173
Set id: e55f6111-c93f-26d0-e053-2995a90ae173
Version: 1
Effective Time: 20220803
 
Hahnemann Laboratories, INC.