NIOBIUM MURIATICUM pellet
Niobium Muriaticum by
Drug Labeling and Warnings
Niobium Muriaticum 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
NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4134 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4134-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 2 NDC: 37662-4134-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 3 NDC: 37662-4134-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 4 NDC: 37662-4134-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4129 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4129-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 2 NDC: 37662-4129-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 3 NDC: 37662-4129-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4130 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4130-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 2 NDC: 37662-4130-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 3 NDC: 37662-4130-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 4 NDC: 37662-4130-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4131 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4131-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 2 NDC: 37662-4131-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 3 NDC: 37662-4131-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 4 NDC: 37662-4131-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4132 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4132-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 2 NDC: 37662-4132-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 3 NDC: 37662-4132-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 4 NDC: 37662-4132-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4128 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4128-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 2 NDC: 37662-4128-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 3 NDC: 37662-4128-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4133 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4133-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 2 NDC: 37662-4133-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/09/2023 3 NDC: 37662-4133-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 4 NDC: 37662-4133-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 NIOBIUM MURIATICUM
niobium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4135 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIOBIUM PENTACHLORIDE (UNII: 9S1BC7865F) (NIOBIUM - UNII:05175J654G) NIOBIUM PENTACHLORIDE 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: 37662-4135-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/09/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-4129, 37662-4130, 37662-4131, 37662-4132, 37662-4128, 37662-4133, 37662-4134, 37662-4135)
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