ANTIMONIUM TARTARICUM pellet
Antimonium Tartaricum by
Drug Labeling and Warnings
Antimonium Tartaricum 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
ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-040 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-040-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-040-02 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-040-03 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-048 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-048-01 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-044 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-044-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-044-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-044-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 4 NDC: 63545-044-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-045 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-045-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-045-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-045-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 4 NDC: 63545-045-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-046 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-046-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-046-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-046-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 4 NDC: 63545-046-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-047 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-047-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-047-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-047-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 4 NDC: 63545-047-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-042 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-042-01 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-042-02 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-042-03 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 4 NDC: 63545-042-04 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-043 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-043-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-043-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-043-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 4 NDC: 63545-043-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 ANTIMONIUM TARTARICUM
antimonium tartaricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-041 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY CATION (3+) 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: 63545-041-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/15/2021 2 NDC: 63545-041-02 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 3 NDC: 63545-041-03 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/15/2021 Labeler - HAHNEMANN LABORATORIES, INC (147098081) Registrant - HAHNEMANN LABORATORIES, INC (147098081)
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