Natrum Oxydatum by Hahnemann Laboratories, INC. NATRUM OXYDATUM pellet
Natrum Oxydatum by
Drug Labeling and Warnings
Natrum Oxydatum 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 OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3848 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM 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: 37662-3848-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 2 NDC: 37662-3848-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 3 NDC: 37662-3848-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 NATRUM OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3854 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM 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: 37662-3854-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 2 NDC: 37662-3854-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 3 NDC: 37662-3854-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 4 NDC: 37662-3854-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 NATRUM OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3849 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM 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: 37662-3849-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 2 NDC: 37662-3849-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 3 NDC: 37662-3849-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 NATRUM OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3850 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM 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: 37662-3850-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 2 NDC: 37662-3850-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 3 NDC: 37662-3850-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 4 NDC: 37662-3850-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 NATRUM OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3853 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM 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: 37662-3853-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 2 NDC: 37662-3853-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 3 NDC: 37662-3853-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 4 NDC: 37662-3853-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 NATRUM OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3851 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM 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: 37662-3851-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 2 NDC: 37662-3851-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 3 NDC: 37662-3851-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 4 NDC: 37662-3851-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 NATRUM OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3852 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM 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: 37662-3852-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 2 NDC: 37662-3852-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/29/2023 3 NDC: 37662-3852-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 4 NDC: 37662-3852-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 NATRUM OXYDATUM
natrum oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-3855 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM OXIDE (UNII: 3075U8R23D) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CATION 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: 37662-3855-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/29/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-3848, 37662-3849, 37662-3850, 37662-3851, 37662-3852, 37662-3853, 37662-3854, 37662-3855)
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