NATRUM SALICYLICUM- natrum salicylicum 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 Salicylicum 6C 5gNatrum Salicylicum 6C 30gNatrum Salicylicum 6C 100gNatrum Salicylicum 12C 5gNatrum Salicylicum 12C 30gNatrum Salicylicum 12C 100gNatrum Salicylicum 30C 1gNatrum Salicylicum 30C 5gNatrum Salicylicum 30C 30gNatrum Salicylicum 30C 100gNatrum Salicylicum 100C 1gNatrum Salicylicum 100C 5gNatrum Salicylicum 100C 30gNatrum Salicylicum 100C 100gNatrum Salicylicum 200C 1gNatrum Salicylicum 200C 5gNatrum Salicylicum 200C 30gNatrum Salicylicum 200C 100gNatrum Salicylicum 500C 1gNatrum Salicylicum 500C 5gNatrum Salicylicum 500C 30gNatrum Salicylicum 500C 100gNatrum Salicylicum 1M 1gNatrum Salicylicum 1M 5gNatrum Salicylicum 1M 30gNatrum Salicylicum 1M 100g

NATRUM SALICYLICUM 
natrum salicylicum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1148
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE12 [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:37662-1148-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
2NDC:37662-1148-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
3NDC:37662-1148-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/02/2022
NATRUM SALICYLICUM 
natrum salicylicum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1149
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE30 [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:37662-1149-180 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
2NDC:37662-1149-2200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
3NDC:37662-1149-31200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
4NDC:37662-1149-44000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/02/2022
NATRUM SALICYLICUM 
natrum salicylicum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1150
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE100 [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:37662-1150-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
2NDC:37662-1150-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
3NDC:37662-1150-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
4NDC:37662-1150-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/02/2022
NATRUM SALICYLICUM 
natrum salicylicum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1152
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE500 [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:37662-1152-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
2NDC:37662-1152-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
3NDC:37662-1152-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
4NDC:37662-1152-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/02/2022
NATRUM SALICYLICUM 
natrum salicylicum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1151
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE200 [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:37662-1151-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
2NDC:37662-1151-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
3NDC:37662-1151-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
4NDC:37662-1151-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/02/2022
NATRUM SALICYLICUM 
natrum salicylicum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1153
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE1 [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:37662-1153-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
2NDC:37662-1153-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
3NDC:37662-1153-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
4NDC:37662-1153-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/02/2022
NATRUM SALICYLICUM 
natrum salicylicum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-1147
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE6 [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:37662-1147-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product08/02/2022
2NDC:37662-1147-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
3NDC:37662-1147-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/02/2022
Labeler - Hahnemann Laboratories, INC. (147098081)
Establishment
NameAddressID/FEIBusiness Operations
Hahnemann Laboratories, INC.147098081manufacture(37662-1147, 37662-1148, 37662-1149, 37662-1150, 37662-1151, 37662-1152, 37662-1153)

Revised: 8/2022
Document Id: e5494923-4ec0-46d4-e053-2a95a90a0161
Set id: e5494923-4ebf-46d4-e053-2a95a90a0161
Version: 1
Effective Time: 20220802
 
Hahnemann Laboratories, INC.