AMMONIUM CARBONICUM pellet
Ammonium Carbonicum by
Drug Labeling and Warnings
Ammonium Carbonicum 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 CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3611 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3611-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3611-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3611-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 4 NDC: 37662-3611-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3615 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3615-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3615-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3615-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 4 NDC: 37662-3615-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3613 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3613-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3613-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3613-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 4 NDC: 37662-3613-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3614 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3614-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3614-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3614-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 4 NDC: 37662-3614-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3609 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3609-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3609-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3609-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3610 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3610-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3610-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3610-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 4 NDC: 37662-3610-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3612 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3612-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3612-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3612-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 4 NDC: 37662-3612-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3608 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 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: 37662-3608-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2023 2 NDC: 37662-3608-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 3 NDC: 37662-3608-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-3608, 37662-3609, 37662-3610, 37662-3611, 37662-3612, 37662-3613, 37662-3614, 37662-3615)
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.