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

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Pancreapar

Energique, Inc.
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Hydrastis Canadensis 3X, Syzygium Jambolanum 3X, Glandula Suprarenalis Suis 6X, Pancreas Suis 6X, Pituitary (Suis) 6X, Phaseolus 9X, Aceticum Acidum 12X, Lacticum Acidum 12X, Phosphoricum Acidum 12X, Phosphorus 12X, Uranium Nitricum 12X

INDICATIONS

For temporary relief of thirst, weakness and feebleness with weight loss, frequent urination, weakness and fatigue with lethargy.

**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 thirst, weakness and feebleness with weight loss, frequent urination, weakness and fatigue with lethargy.

**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

PANCREAPAR

1 fl. oz. (30 ml)

Pancreapar

Pancreapar

Hydrastis Canadensis, Syzygium Jambolanum, Glandula Suprarenalis Suis, Pancreas Suis, Pituitary, Phaseolus LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44911-0075
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GOLDENSEAL GOLDENSEAL 3 [hp_X]
SYZYGIUM CUMINI SEED SYZYGIUM CUMINI SEED 3 [hp_X]
SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND 6 [hp_X]
SUS SCROFA PANCREAS SUS SCROFA PANCREAS 6 [hp_X]
SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND 6 [hp_X]
KIDNEY BEAN KIDNEY BEAN 9 [hp_X]
ACETIC ACID 12 [hp_X]
LACTIC ACID 12 [hp_X]
phosphoric acid PHOSPHORIC ACID 12 [hp_X]
PHOSPHORUS PHOSPHORUS 12 [hp_X]
URANYL NITRATE HEXAHYDRATE URANIUM CATION (6+) 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44911-0075-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-04-11


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