ERBIUM METALLICUM pellet
Erbium Metallicum by
Drug Labeling and Warnings
Erbium Metallicum 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
ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0696 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0696-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 2 NDC: 37662-0696-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 3 NDC: 37662-0696-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0701 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0701-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 2 NDC: 37662-0701-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 3 NDC: 37662-0701-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 4 NDC: 37662-0701-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0702 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0702-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0700 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0700-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 2 NDC: 37662-0700-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 3 NDC: 37662-0700-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 4 NDC: 37662-0700-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0698 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0698-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 2 NDC: 37662-0698-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 3 NDC: 37662-0698-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 4 NDC: 37662-0698-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0695 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0695-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 2 NDC: 37662-0695-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 3 NDC: 37662-0695-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0697 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0697-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 2 NDC: 37662-0697-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 3 NDC: 37662-0697-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 4 NDC: 37662-0697-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 ERBIUM METALLICUM
erbium metallicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0699 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM (UNII: 77B218D3YE) (ERBIUM - UNII:77B218D3YE) ERBIUM 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: 37662-0699-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 2 NDC: 37662-0699-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/04/2022 3 NDC: 37662-0699-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 4 NDC: 37662-0699-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/04/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-0695, 37662-0696, 37662-0697, 37662-0698, 37662-0699, 37662-0700, 37662-0701, 37662-0702)
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