Label: KALI OXALICUM pellet
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NDC Code(s):
37662-3745-1,
37662-3745-2,
37662-3745-3,
37662-3746-1, view more37662-3746-2, 37662-3746-3, 37662-3747-1, 37662-3747-2, 37662-3747-3, 37662-3747-4, 37662-3748-1, 37662-3748-2, 37662-3748-3, 37662-3748-4, 37662-3749-1, 37662-3749-2, 37662-3749-3, 37662-3749-4, 37662-3750-1, 37662-3750-2, 37662-3750-3, 37662-3750-4, 37662-3751-1, 37662-3751-2, 37662-3751-3, 37662-3751-4, 37662-3752-1
- 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 August 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
-
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)
