NATRUM ARSENICICUM pellet
Natrum Arsenicicum by
Drug Labeling and Warnings
Natrum Arsenicicum 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
NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1853 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1853-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1853-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1853-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1854 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1854-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1854-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1854-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1855 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1855-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1855-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1855-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 4 NDC: 37662-1855-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1856 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1856-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1856-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1856-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 4 NDC: 37662-1856-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1861 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1861-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1857 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1857-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1857-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1857-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 4 NDC: 37662-1857-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1858 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1858-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1858-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1858-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 4 NDC: 37662-1858-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1859 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1859-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1859-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1859-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 4 NDC: 37662-1859-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 NATRUM ARSENICICUM
natrum arsenicicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-1860 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W) (ARSENATE ION - UNII:G1DBI405OK) SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 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: 37662-1860-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 2 NDC: 37662-1860-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/07/2022 3 NDC: 37662-1860-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 4 NDC: 37662-1860-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/07/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-1853, 37662-1854, 37662-1855, 37662-1856, 37662-1857, 37662-1858, 37662-1859, 37662-1860, 37662-1861)
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