AMMONIUM PHOSPHORICUM pellet
Ammonium Phosphoricum by
Drug Labeling and Warnings
Ammonium Phosphoricum 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
AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3636 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3636-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3636-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3636-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3636-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3633 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3633-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3633-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3633-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3634 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3634-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3634-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3634-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3634-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3638 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3638-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3638-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3638-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3638-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3632 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3632-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3632-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3632-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3635 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3635-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3635-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3635-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3635-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3637 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3637-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3637-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3637-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3637-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3639 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) AMMONIUM PHOSPHATE, DIBASIC 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: 37662-3639-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3639-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3639-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3639-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-3633, 37662-3634, 37662-3632, 37662-3635, 37662-3636, 37662-3637, 37662-3638, 37662-3639)
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