Label: AURUM MURIATICUM NATRONATUM pellet
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NDC Code(s):
37662-2726-1,
37662-2726-2,
37662-2726-3,
37662-2727-1, view more37662-2727-2, 37662-2727-3, 37662-2728-1, 37662-2728-2, 37662-2728-3, 37662-2728-4, 37662-2729-1, 37662-2729-2, 37662-2729-3, 37662-2729-4, 37662-2730-1, 37662-2730-2, 37662-2730-3, 37662-2730-4, 37662-2731-1, 37662-2731-2, 37662-2731-3, 37662-2731-4, 37662-2732-1, 37662-2732-2, 37662-2732-3, 37662-2732-4, 37662-2733-1, 37662-2733-2, 37662-2733-3, 37662-2733-4
- 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 February 24, 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
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INGREDIENTS AND APPEARANCE
AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2726 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2726-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2726-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2726-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2729 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2729-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2729-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2729-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 4 NDC:37662-2729-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2732 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2732-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2732-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2732-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 4 NDC:37662-2732-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2728 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2728-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2728-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2728-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 4 NDC:37662-2728-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2731 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2731-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2731-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2731-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 4 NDC:37662-2731-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2733 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2733-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2733-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2733-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 4 NDC:37662-2733-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2727 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2727-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2727-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2727-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 AURUM MURIATICUM NATRONATUM
aurum muriaticum natronatum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2730 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE 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:37662-2730-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 2 NDC:37662-2730-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/28/2023 3 NDC:37662-2730-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 4 NDC:37662-2730-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/28/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-2726, 37662-2727, 37662-2728, 37662-2729, 37662-2730, 37662-2731, 37662-2732, 37662-2733)
