Label: KALI SULPHURICUM pellet
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NDC Code(s):
37662-2372-1,
37662-2372-2,
37662-2372-3,
37662-2373-1, view more37662-2373-2, 37662-2373-3, 37662-2374-1, 37662-2374-2, 37662-2374-3, 37662-2374-4, 37662-2375-1, 37662-2375-2, 37662-2375-3, 37662-2375-4, 37662-2376-1, 37662-2376-2, 37662-2376-3, 37662-2376-4, 37662-2377-1, 37662-2377-2, 37662-2377-3, 37662-2377-4, 37662-2378-1, 37662-2378-2, 37662-2378-3, 37662-2378-4, 37662-2379-1, 37662-2379-2, 37662-2379-3, 37662-2379-4
- Packager: Hahnemann Laboratories, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated January 17, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
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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)
