LITHIUM CARBONICUM pellet
Lithium Carbonicum by
Drug Labeling and Warnings
Lithium 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
LITHIUM CARBONICUM
lithium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0939 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM 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: 37662-0939-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 2 NDC: 37662-0939-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 3 NDC: 37662-0939-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 4 NDC: 37662-0939-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2022 LITHIUM CARBONICUM
lithium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0936 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM 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: 37662-0936-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 2 NDC: 37662-0936-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 3 NDC: 37662-0936-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2022 LITHIUM CARBONICUM
lithium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0940 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM 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: 37662-0940-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 2 NDC: 37662-0940-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 3 NDC: 37662-0940-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 4 NDC: 37662-0940-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2022 LITHIUM CARBONICUM
lithium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0937 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM 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: 37662-0937-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 2 NDC: 37662-0937-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 3 NDC: 37662-0937-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 4 NDC: 37662-0937-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2022 LITHIUM CARBONICUM
lithium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0938 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM 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: 37662-0938-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 2 NDC: 37662-0938-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 3 NDC: 37662-0938-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 4 NDC: 37662-0938-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2022 LITHIUM CARBONICUM
lithium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0935 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM 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: 37662-0935-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 2 NDC: 37662-0935-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 3 NDC: 37662-0935-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2022 LITHIUM CARBONICUM
lithium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0941 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM 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: 37662-0941-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 2 NDC: 37662-0941-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/15/2022 3 NDC: 37662-0941-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 4 NDC: 37662-0941-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-0935, 37662-0936, 37662-0937, 37662-0938, 37662-0939, 37662-0940, 37662-0941)
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.