Thyrostat description, usages, side effects, indications, overdosage, supplying and lots more!

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Thyrostat

Energique, Inc.
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Fucus Vesiculosus 3X, Spongia Tosta 3X, Pituitaria Glandula (Suis) 6X, Thyroidinum (Suis) 6X, Arsenicum Iodatum 12X, Baryta Carbonica 12X, Calcarea Carbonica 12X, Iodium 12X, Lycopus Virginicus 12X, Natrum Muriaticum 12X,

INDICATIONS

For temporary relief of difficulty swallowing, flushed face, glaring eyes, excited mental state or nervousness.

These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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.

DIRECTIONS

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

INACTIVE INGREDIENTS

Demineralized water, 20% Ethanol.

KEEP OUT OF REACH OF CHILDREN

In case of overdose, get medical help or contact a Poison Control Center right away.

INDICATIONS AND USAGE

For temporary relief of difficulty swallowing, flushed face, glaring eyes, excited mental state or nervousness.

These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

QUESTIONS

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579

800-869-8078

ENERGIQUE

since 1987

HOMEOPATHIC REMEDY

THYROSTAT

1 fl. oz. (30 ml)

Thyrostat

Thyrostat

Fucus Vesiculosus, Spongia Tosta, Pituitaria Glandula, Thyroidinum, Arsenicum Iodatum, Baryta Carbonica LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44911-0058
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FUCUS VESICULOSUS FUCUS VESICULOSUS 3 [hp_X]
SPONGIA OFFICINALIS SKELETON, ROASTED SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X]
SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND 6 [hp_X]
SUS SCROFA THYROID SUS SCROFA THYROID 6 [hp_X]
ARSENIC TRIIODIDE ARSENIC TRIIODIDE 12 [hp_X]
BARIUM CARBONATE BARIUM CATION 12 [hp_X]
OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]
Iodine IODINE 12 [hp_X]
Lycopus Virginicus LYCOPUS VIRGINICUS 12 [hp_X]
SODIUM CHLORIDE 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44911-0058-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-12-03


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