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

Pancreapar

Apotheca Company

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Pancreapar



FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS:  Hydrastis canadensis 3X, Syzygium jambolanum 3X, Glandula suprarenalis 6X, Pancreas 6X, Pituitaria glandula 6X, Phaseolus 9X, Aceticum acidum 12X, Lacticum acidum 12X, Phosphoricum acidum 12X, Phosphorus 12X, Uranium nitricum 12X.


Purpose

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


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.




SUGGESTED USE:  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.


Uses

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

Dist by  Energique, Inc.

201 Apple Blvd.

Woodbine, I 51579

800-869-8078

ENERGIQUE

PANCREAPAR

Homeopathic Remedy

1 fl. oz. (30 ml)

Pancreapar

Hydrastis canadensis, Syzgium jambolanum, Glandula suprarenalis, Pancreas, Pituitaris glandula Phaseolus, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57520-0381
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]
KIDNEY BEAN KIDNEY BEAN 9 [hp_X]
ACETIC ACID 12 [hp_X]
LACTIC ACID, DL- LACTIC ACID, DL- 12 [hp_X]
phosphoric acid PHOSPHORIC ACID 12 [hp_X]
PHOSPHORUS PHOSPHORUS 12 [hp_X]
URANYL NITRATE HEXAHYDRATE URANIUM CATION (6+) 12 [hp_X]
SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND 6 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57520-0381-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2010-05-07


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Be sure to consult your doctor before taking any medication!
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