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

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Hypothalmupar

Energique, Inc.
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Aralia Quinquefolia 3X, Ginkgo Biloba 3X, Hydrocotyle Asiatica 3X, Brain (Suis) 6X, Hypothalamus (Suis) 6X, Pituitaria Glandula (Suis) 6X, Phosphorus 12X, Silicea 12X

INDICATIONS

For temporary relief of weakness, exhaustion and vertigo, and difficult mental concentration.

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 weakness, exhaustion and vertigo, and difficult mental concentration.

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

HYPOTHALMUPAR

1 fl. oz. (30 ml)

Hypothalmupar

Hypothalmupar

Aralia Quinquefolia, Ginkgo Biloba, Hydrocotyle Asiatica, Brain, Hypothalamus, Pituitaria Glandula, Phosphorus, Silicea LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44911-0069
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AMERICAN GINSENG American Ginseng 3 [hp_X]
GINKGO 3 [hp_X]
CENTELLA ASIATICA 3 [hp_X]
PORK BRAIN PORK BRAIN 6 [hp_X]
SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS 6 [hp_X]
SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND 6 [hp_X]
PHOSPHORUS PHOSPHORUS 12 [hp_X]
SILICON DIOXIDE 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44911-0069-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-01-02


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Be sure to consult your doctor before taking any medication!
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