Kali Sulphuricum by Hahnemann Laboratories, INC. KALI SULPHURICUM pellet
Kali Sulphuricum by
Drug Labeling and Warnings
Kali Sulphuricum by is a Homeopathic medication manufactured, distributed, or labeled by 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
KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2373 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 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: 37662-2373-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2373-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2373-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2376 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 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: 37662-2376-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2376-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2376-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 4 NDC: 37662-2376-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2372 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 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: 37662-2372-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2372-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2372-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2378 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 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: 37662-2378-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2378-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2378-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 4 NDC: 37662-2378-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2379 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 10 [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: 37662-2379-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2379-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2379-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 4 NDC: 37662-2379-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2377 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 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: 37662-2377-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2377-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2377-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 4 NDC: 37662-2377-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2374 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 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: 37662-2374-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2374-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2374-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 4 NDC: 37662-2374-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 KALI SULPHURICUM
kali sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2375 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 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: 37662-2375-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 2 NDC: 37662-2375-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/17/2023 3 NDC: 37662-2375-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 4 NDC: 37662-2375-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/17/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-2372, 37662-2373, 37662-2374, 37662-2375, 37662-2376, 37662-2377, 37662-2378, 37662-2379)
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