Terrestristat

Terrestristat is an FDA drug label for the active ingredient ALFALFA, AVENA SATIVA, FUCUS VESICULOSUS, ARALIA QUINQUEFOLIA, NATRUM CARBONICUM, THYROIDINUM (SUIS), CEREBRUM SUIS, PINEAL GLAND (SUIS), RHODODENDRON CHRYSANTHUM, AGATE, ARGENTUM NITRICUM, CADMIUM IODATUM, CALCAREA PHOSPHORICA, COFFEA CRUDA, CUPRUM METALLICUM, MERCURIUS CORROSIVUS, PHOSPHORICUM ACIDUM, PHOSPHORUS, QUARTZ, SILICEA, STRONTIUM CARBONICUM, RADIUM BROMATUM, CARCINOSIN, TARENTULA CUBENSIS, X-RAY, HOLMIUM METALLICUM, URANIUM NITRICUM. manufactured by Energique, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231117.

Generic: ALFALFA, AVENA SATIVA, FUCUS VESICULOSUS, ARALIA QUINQUEFOLIA, NATRUM CARBONICUM, THYROIDINUM (SUIS), CEREBRUM SUIS, PINEAL GLAND (SUIS), RHODODENDRON CHRYSANTHUM, AGATE, ARGENTUM NITRICUM, CADMIUM IODATUM, CALCAREA PHOSPHORICA, COFFEA CRUDA, CUPRUM METALLICUM, MERCURIUS CORROSIVUS, PHOSPHORICUM ACIDUM, PHOSPHORUS, QUARTZ, SILICEA, STRONTIUM CARBONICUM, RADIUM BROMATUM, CARCINOSIN, TARENTULA CUBENSIS, X-RAY, HOLMIUM METALLICUM, URANIUM NITRICUM.

Manufacturer: Energique, Inc.

Product Type: HUMAN OTC DRUG

Route: ORAL

Dosage Form:

NDC: 44911-0677

Application:

Effective: 20231117

Active Ingredients: ACTIVE INGREDIENTS: (in each drop): 3.98% of Aralia Quinquefolia 6X, Argentum Nitricum 12X, Cadmium Iodatum 12X, Calcarea Phosphorica 12X, Carcinosin 30X, Cerebrum 8X, Coffea Cruda 12X, Cuprum Metallicum 12X, Holmium Metallicum 12C, Mercurius Corrosivus 12X, Natrum Carbonicum 6X, Phosphorus 12X, Phosphoricum Acidum 12X, Pineal Gland 8X, Quartz 12X, Radium Bromatum 16X, Rhododendron Chrysanthum 10X, Silicea 12X, Strontium Carbonicum 12X, Tarentula Cubensis 30X, Thyroidinum 6X, Uranium Nitricum 15C, X-Ray 30X, 60X, 200X; 0.10% of Agate 12X, Alfalfa 3X, Avena Sativa 3X, Fucus Vesiculosus 3X,

Indications & Usage

INDICATIONS: May temporarily relieve nervousness, anxiety, restlessness, weakness, trembling, numbness, and skin eruptions and cracking.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Contraindications

Not available.

Warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Adverse Reactions

Not available.

More from same ingredient

No related products.