Thyroveev Hyperthyroid Symptom Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Antimony Trisulfide; Antimony Triiodide; Sodium Chloride; Silver Iodide; Spongilla Lacustris; Bromine; Oyster Shell Calcium Carbonate, Crude; Calcium Iodide; Cobaltous Nitrate Hexahydrate; Ferrous Iodide; Fucus Vesiculosus; Gelsemium Sempervirens Root; Gentianella Amarella Flower; Goldenseal; Strychnos Ignatii Seed; Iodine; Potassium Iodide; Calcium Hexafluorosilicate; Sodium Bromide; Thyroid, Unspecified; Parathyroid Hormone; Phosphoric Acid; Rosmarinus Officinalis Flowering Top; Sulfur Iodide.
Product ID | 49726-025_7df183c1-5f81-1a16-e053-2991aa0a2223 |
NDC | 49726-025 |
Product Type | Human Otc Drug |
Proprietary Name | Thyroveev Hyperthyroid Symptom Relief |
Generic Name | Antimonium Crudum, Antimonium Iodatum, Aqua Marina, Argentum Iodatum, Badiaga, Bromium, Calcarea Carbonica, Calcarea Iodata, Cobaltum Nitricum, Ferrum Iodatum, Fucus, Gelsemium, Gentianella Amarella Flos, Hydrastis, Ignatia, Iodium, Kali Iodatum, Lapis, Natrum Bromatum, Natrum Muriaticum, Parathormonum, Phosphoricum Acidum, Rosmarinus, Sulphur Iodatum, Thyroidinum |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2012-08-15 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Hello Life, Inc. |
Substance Name | ANTIMONY TRISULFIDE; ANTIMONY TRIIODIDE; SODIUM CHLORIDE; SILVER IODIDE; SPONGILLA LACUSTRIS; BROMINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM IODIDE; COBALTOUS NITRATE HEXAHYDRATE; FERROUS IODIDE; FUCUS VESICULOSUS; GELSEMIUM SEMPERVIRENS ROOT; GENTIANELLA AMARELLA FLOWER; GOLDENSEAL; STRYCHNOS IGNATII SEED; IODINE; POTASSIUM IODIDE; CALCIUM HEXAFLUOROSILICATE; SODIUM BROMIDE; THYROID, UNSPECIFIED; PARATHYROID HORMONE; PHOSPHORIC ACID; ROSMARINUS OFFICINALIS FLOWERING TOP; SULFUR IODIDE |
Active Ingredient Strength | 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2012-08-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-08-15 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ANTIMONY TRISULFIDE | 10 [hp_X]/59mL |
SPL SET ID: | 2427ad19-c6a7-4323-98dc-60fabcae4d6a |
Manufacturer | |
UNII |