MOLYBDENUM PHOSPHORATUM pellet
Molybdenum Phosphoratum by
Drug Labeling and Warnings
Molybdenum Phosphoratum 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
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3888 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3888-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 2 NDC: 37662-3888-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 3 NDC: 37662-3888-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3892 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3892-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 2 NDC: 37662-3892-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 3 NDC: 37662-3892-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 4 NDC: 37662-3892-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3895 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3895-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3894 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3894-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 2 NDC: 37662-3894-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 3 NDC: 37662-3894-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 4 NDC: 37662-3894-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3893 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3893-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 2 NDC: 37662-3893-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 3 NDC: 37662-3893-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 4 NDC: 37662-3893-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3890 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3890-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 2 NDC: 37662-3890-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 3 NDC: 37662-3890-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 4 NDC: 37662-3890-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3889 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3889-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 2 NDC: 37662-3889-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 3 NDC: 37662-3889-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 MOLYBDENUM PHOSPHORATUM
molybdenum phosphoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3891 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHOMOLYBDIC ACID (UNII: RN225F04V1) (PHOSPHOMOLYBDIC ACID - UNII:RN225F04V1) PHOSPHOMOLYBDIC ACID 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: 37662-3891-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 2 NDC: 37662-3891-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/08/2023 3 NDC: 37662-3891-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 4 NDC: 37662-3891-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-3888, 37662-3889, 37662-3890, 37662-3891, 37662-3892, 37662-3893, 37662-3894, 37662-3895)
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