NICCOLUM SULPHURICUM pellet
Niccolum Sulphuricum by
Drug Labeling and Warnings
Niccolum Sulphuricum by is a Homeopathic medication manufactured, distributed, or labeled by Hahnemann Laboratories, INC., Hahnemann Laboratories. INC.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- 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
-
INGREDIENTS AND APPEARANCE
NICCOLUM SULPHURICUM
niccolum sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1163 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE 12 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-1163-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 2 NDC: 37662-1163-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 3 NDC: 37662-1163-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/02/2022 NICCOLUM SULPHURICUM
niccolum sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1168 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE 1 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-1168-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 2 NDC: 37662-1168-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 3 NDC: 37662-1168-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 4 NDC: 37662-1168-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/02/2022 NICCOLUM SULPHURICUM
niccolum sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1164 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE 30 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-1164-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 2 NDC: 37662-1164-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 3 NDC: 37662-1164-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 4 NDC: 37662-1164-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/02/2022 NICCOLUM SULPHURICUM
niccolum sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1165 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE 100 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-1165-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 2 NDC: 37662-1165-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 3 NDC: 37662-1165-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 4 NDC: 37662-1165-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/02/2022 NICCOLUM SULPHURICUM
niccolum sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1162 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-1162-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 2 NDC: 37662-1162-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 3 NDC: 37662-1162-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/02/2022 NICCOLUM SULPHURICUM
niccolum sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1166 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE 200 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-1166-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 2 NDC: 37662-1166-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 3 NDC: 37662-1166-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 4 NDC: 37662-1166-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/02/2022 NICCOLUM SULPHURICUM
niccolum sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1167 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE 500 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-1167-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 2 NDC: 37662-1167-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/02/2022 3 NDC: 37662-1167-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 4 NDC: 37662-1167-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/02/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories. INC. 147098081 manufacture(37662-1163, 37662-1164, 37662-1162, 37662-1165, 37662-1166, 37662-1167, 37662-1168)
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