RUBIDIUM MURIATICUM pellet
Rubidium Muriaticum by
Drug Labeling and Warnings
Rubidium 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
RUBIDIUM MURIATICUM
rubidium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4027 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM CHLORIDE (UNII: N3SHC5273S) (RUBIDIUM CATION - UNII:PR87B22TGJ) RUBIDIUM CHLORIDE 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: 37662-4027-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 2 NDC: 37662-4027-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 3 NDC: 37662-4027-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 4 NDC: 37662-4027-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2023 RUBIDIUM MURIATICUM
rubidium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4025 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM CHLORIDE (UNII: N3SHC5273S) (RUBIDIUM CATION - UNII:PR87B22TGJ) RUBIDIUM CHLORIDE 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: 37662-4025-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 2 NDC: 37662-4025-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 3 NDC: 37662-4025-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2023 RUBIDIUM MURIATICUM
rubidium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4026 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM CHLORIDE (UNII: N3SHC5273S) (RUBIDIUM CATION - UNII:PR87B22TGJ) RUBIDIUM CHLORIDE 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: 37662-4026-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 2 NDC: 37662-4026-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 3 NDC: 37662-4026-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 4 NDC: 37662-4026-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2023 RUBIDIUM MURIATICUM
rubidium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4028 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM CHLORIDE (UNII: N3SHC5273S) (RUBIDIUM CATION - UNII:PR87B22TGJ) RUBIDIUM CHLORIDE 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: 37662-4028-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 2 NDC: 37662-4028-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 3 NDC: 37662-4028-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 4 NDC: 37662-4028-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2023 RUBIDIUM MURIATICUM
rubidium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4024 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM CHLORIDE (UNII: N3SHC5273S) (RUBIDIUM CATION - UNII:PR87B22TGJ) RUBIDIUM CHLORIDE 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: 37662-4024-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 2 NDC: 37662-4024-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 3 NDC: 37662-4024-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2023 RUBIDIUM MURIATICUM
rubidium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4029 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM CHLORIDE (UNII: N3SHC5273S) (RUBIDIUM CATION - UNII:PR87B22TGJ) RUBIDIUM CHLORIDE 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: 37662-4029-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 2 NDC: 37662-4029-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 3 NDC: 37662-4029-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 4 NDC: 37662-4029-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2023 RUBIDIUM MURIATICUM
rubidium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4030 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM CHLORIDE (UNII: N3SHC5273S) (RUBIDIUM CATION - UNII:PR87B22TGJ) RUBIDIUM CHLORIDE 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: 37662-4030-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 2 NDC: 37662-4030-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/27/2023 3 NDC: 37662-4030-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 4 NDC: 37662-4030-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/27/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-4024, 37662-4025, 37662-4026, 37662-4027, 37662-4028, 37662-4029, 37662-4030)
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