Kali Oxalicum by Hahnemann Laboratories, INC. KALI OXALICUM pellet
Kali Oxalicum by
Drug Labeling and Warnings
Kali Oxalicum 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 OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3750 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 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: 37662-3750-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 2 NDC: 37662-3750-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 3 NDC: 37662-3750-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 4 NDC: 37662-3750-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 KALI OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3749 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 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: 37662-3749-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 2 NDC: 37662-3749-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 3 NDC: 37662-3749-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 4 NDC: 37662-3749-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 KALI OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3752 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 1 [hp_Q] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 1mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-3752-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 KALI OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3746 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 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: 37662-3746-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 2 NDC: 37662-3746-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 3 NDC: 37662-3746-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 KALI OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3748 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 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: 37662-3748-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 2 NDC: 37662-3748-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 3 NDC: 37662-3748-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 4 NDC: 37662-3748-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 KALI OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3747 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 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: 37662-3747-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 2 NDC: 37662-3747-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 3 NDC: 37662-3747-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 4 NDC: 37662-3747-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 KALI OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3751 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 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: 37662-3751-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 2 NDC: 37662-3751-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 3 NDC: 37662-3751-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 4 NDC: 37662-3751-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 KALI OXALICUM
kali oxalicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3745 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM OXALATE (UNII: LC7F2W7I5B) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM OXALATE 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: 37662-3745-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/17/2023 2 NDC: 37662-3745-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 3 NDC: 37662-3745-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/17/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-3745, 37662-3746, 37662-3747, 37662-3748, 37662-3749, 37662-3750, 37662-3751, 37662-3752)
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