Label: NIOBIUM OXYDATUM pellet
-
NDC Code(s):
37662-3785-1,
37662-3785-2,
37662-3785-3,
37662-3786-1, view more37662-3786-2, 37662-3786-3, 37662-3787-1, 37662-3787-2, 37662-3787-3, 37662-3787-4, 37662-3788-1, 37662-3788-2, 37662-3788-3, 37662-3788-4, 37662-3789-1, 37662-3789-2, 37662-3789-3, 37662-3789-4, 37662-3790-1, 37662-3790-2, 37662-3790-3, 37662-3790-4, 37662-3791-1, 37662-3791-2, 37662-3791-3, 37662-3791-4, 37662-3792-1
- Packager: Hahnemann Laboratories, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated August 21, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3786 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3786-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 2 NDC:37662-3786-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 3 NDC:37662-3786-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3792 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3792-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3791 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3791-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 2 NDC:37662-3791-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 3 NDC:37662-3791-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 4 NDC:37662-3791-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3788 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3788-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 2 NDC:37662-3788-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 3 NDC:37662-3788-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 4 NDC:37662-3788-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3789 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3789-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 2 NDC:37662-3789-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 3 NDC:37662-3789-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 4 NDC:37662-3789-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3787 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3787-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 2 NDC:37662-3787-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 3 NDC:37662-3787-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 4 NDC:37662-3787-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3785 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3785-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 2 NDC:37662-3785-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 3 NDC:37662-3785-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 NIOBIUM OXYDATUM
niobium oxydatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-3790 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM NIOBIUM(V) OXIDE (UNII: 5QYT6674V4) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM NIOBIUM(V) OXIDE 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:37662-3790-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 2 NDC:37662-3790-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/21/2023 3 NDC:37662-3790-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 4 NDC:37662-3790-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-3786, 37662-3787, 37662-3785, 37662-3788, 37662-3789, 37662-3790, 37662-3791, 37662-3792)
