ANTIMONIUM OXYDATUM pellet
Antimonium Oxydatum by
Drug Labeling and Warnings
Antimonium Oxydatum 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 OXYDATUM
antimonium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-036 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRIOXIDE (UNII: P217481X5E) (ANTIMONY TRIOXIDE - UNII:P217481X5E) ANTIMONY TRIOXIDE 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: 63545-036-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 2 NDC: 63545-036-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 3 NDC: 63545-036-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 4 NDC: 63545-036-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/09/2021 ANTIMONIUM OXYDATUM
antimonium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-034 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRIOXIDE (UNII: P217481X5E) (ANTIMONY TRIOXIDE - UNII:P217481X5E) ANTIMONY TRIOXIDE 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: 63545-034-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 2 NDC: 63545-034-02 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 3 NDC: 63545-034-03 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/09/2021 ANTIMONIUM OXYDATUM
antimonium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-037 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRIOXIDE (UNII: P217481X5E) (ANTIMONY TRIOXIDE - UNII:P217481X5E) ANTIMONY TRIOXIDE 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: 63545-037-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 2 NDC: 63545-037-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 3 NDC: 63545-037-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 4 NDC: 63545-037-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/09/2021 ANTIMONIUM OXYDATUM
antimonium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-039 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRIOXIDE (UNII: P217481X5E) (ANTIMONY TRIOXIDE - UNII:P217481X5E) ANTIMONY TRIOXIDE 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: 63545-039-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 2 NDC: 63545-039-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 3 NDC: 63545-039-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 4 NDC: 63545-039-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/09/2021 ANTIMONIUM OXYDATUM
antimonium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-033 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRIOXIDE (UNII: P217481X5E) (ANTIMONY TRIOXIDE - UNII:P217481X5E) ANTIMONY TRIOXIDE 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: 63545-033-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 2 NDC: 63545-033-02 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 3 NDC: 63545-033-03 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/09/2021 ANTIMONIUM OXYDATUM
antimonium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-038 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRIOXIDE (UNII: P217481X5E) (ANTIMONY TRIOXIDE - UNII:P217481X5E) ANTIMONY TRIOXIDE 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: 63545-038-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 2 NDC: 63545-038-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 3 NDC: 63545-038-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 4 NDC: 63545-038-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/09/2021 ANTIMONIUM OXYDATUM
antimonium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 63545-035 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRIOXIDE (UNII: P217481X5E) (ANTIMONY TRIOXIDE - UNII:P217481X5E) ANTIMONY TRIOXIDE 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: 63545-035-01 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 2 NDC: 63545-035-04 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 3 NDC: 63545-035-03 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/09/2021 4 NDC: 63545-035-02 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/09/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/09/2021 Labeler - Hahnemann Laboratories, Inc. (147098081) Registrant - Hahnemann Laboratories, Inc. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, Inc. 147098081 manufacture(63545-033, 63545-034, 63545-035, 63545-036, 63545-037, 63545-038, 63545-039)
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