Label: TERRESTRISTAT (alfalfa, avena sativa, fucus vesiculosus, aralia quinquefolia, natrum carbonicum, thyroidinum (suis), pineal gland- suis, rhododendron chrysanthum, agate, argentum nitricum, cadmium iodatum, calcarea phosphorica, cuprum metallicum, mercurius corrosivus, phosphoricum acidum, phosphorus, quartz, silicea, strontium carbonicum, holmium metallicum, radium bromatum, tarentula cubensis, uranium nitricum, x-ray liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 44911-0522-1 - Packager: Energique, 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 July 27, 2021
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ACTIVE INGREDIENTS:
(in each drop): 4.53% of Aralia Quinquefolia 6X, Argentum Nitricum 12X, Cadmium Iodatum 12X, Calcarea Phosphorica 12X, Cuprum Metallicum 12X, Holmium Metallicum 16X, Mercurius Corrosivus 12X, Natrum Carbonicum 6X, Phosphoricum Acidum 12X, Phosphorus 12X, Pineal Gland (Suis) 8X, Quartz 12X, Radium Bromatum 16X, Rhododendron Chrysanthum 10X, Silicea 12X, Strontium Carbonicum 12X, Tarentula Cubensis 30X, Thyroidinum (Suis) 6X, Uranium Nitricum 30X, X-Ray 30X, 60X, 200X; 0.10% of Agate 12X, Alfalfa 3X, Avena Sativa 3X, Fucus Vesiculosus 3X.
- INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE DISPLAY LABEL:
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INGREDIENTS AND APPEARANCE
TERRESTRISTAT
alfalfa, avena sativa, fucus vesiculosus, aralia quinquefolia, natrum carbonicum, thyroidinum (suis), pineal gland (suis), rhododendron chrysanthum, agate, argentum nitricum, cadmium iodatum, calcarea phosphorica, cuprum metallicum, mercurius corrosivus, phosphoricum acidum, phosphorus, quartz, silicea, strontium carbonicum, holmium metallicum, radium bromatum, tarentula cubensis, uranium nitricum, x-ray liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0522 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALFALFA (UNII: DJO934BRBD) (ALFALFA - UNII:DJO934BRBD) ALFALFA 3 [hp_X] in 1 mL AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (AVENA SATIVA FLOWERING TOP - UNII:MA9CQJ3F7F) AVENA SATIVA FLOWERING TOP 3 [hp_X] in 1 mL FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 3 [hp_X] in 1 mL AMERICAN GINSENG (UNII: 8W75VCV53Q) (AMERICAN GINSENG - UNII:8W75VCV53Q) AMERICAN GINSENG 6 [hp_X] in 1 mL SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D) SODIUM CARBONATE 6 [hp_X] in 1 mL SUS SCROFA THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ) SUS SCROFA THYROID 6 [hp_X] in 1 mL SUS SCROFA PINEAL GLAND (UNII: 050QZ2EDK7) (SUS SCROFA PINEAL GLAND - UNII:050QZ2EDK7) SUS SCROFA PINEAL GLAND 8 [hp_X] in 1 mL RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U) RHODODENDRON AUREUM LEAF 10 [hp_X] in 1 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 12 [hp_X] in 1 mL CADMIUM IODIDE (UNII: 2F2UPU4KCW) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM IODIDE 12 [hp_X] in 1 mL TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 12 [hp_X] in 1 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 12 [hp_X] in 1 mL MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 12 [hp_X] in 1 mL PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 12 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 12 [hp_X] in 1 mL STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (STRONTIUM CATION - UNII:37077S2C93) STRONTIUM CARBONATE 12 [hp_X] in 1 mL HOLMIUM (UNII: W1XX32SQN1) (HOLMIUM - UNII:W1XX32SQN1) HOLMIUM 16 [hp_X] in 1 mL RADIUM BROMIDE (UNII: R74O7T8569) (RADIUM CATION - UNII:05456MVL7T) RADIUM BROMIDE 16 [hp_X] in 1 mL CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823) (CITHARACANTHUS SPINICRUS - UNII:3Y5X6RT823) CITHARACANTHUS SPINICRUS 16 [hp_X] in 1 mL URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7) URANYL NITRATE HEXAHYDRATE 30 [hp_X] in 1 mL ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (ALCOHOL, X-RAY EXPOSED (1000 RAD) - UNII:6PRJ93602P) ALCOHOL, X-RAY EXPOSED (1000 RAD) 30 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44911-0522-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 02/19/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/19/2020 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0522) , api manufacture(44911-0522) , label(44911-0522) , pack(44911-0522)