AMMONIUM MURIATICUM pellet
Ammonium Muriaticum by
Drug Labeling and Warnings
Ammonium 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
AMMONIUM MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3626 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3626-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3626-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3626-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3626-4 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 MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3625 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3625-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3625-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3625-3 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 MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3627 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3627-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3627-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3627-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3627-4 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 MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3629 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3629-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3629-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3629-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3629-4 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 MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3628 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3628-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3628-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3628-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3628-4 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 MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3624 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3624-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3624-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3624-3 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 MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3631 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3631-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3631-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3631-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3631-4 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 MURIATICUM
ammonium muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3630 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 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: 37662-3630-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 2 NDC: 37662-3630-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/13/2023 3 NDC: 37662-3630-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/13/2023 4 NDC: 37662-3630-4 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(37662-3624, 37662-3625, 37662-3626, 37662-3627, 37662-3628, 37662-3629, 37662-3630, 37662-3631)
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