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

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Ultra Pure

Soza Clinic
Soza Clinic

Ultra Pure




FULL PRESCRIBING INFORMATION

Directions: Swirl or shake bottle 5 times prior to use. Adults and children above 10 years old, apply three sprays under the tongue twice daily, upon awakening and before sleeping. Do not eat, drink, or brush your teeth within 5 minutes before or after taking this remedy. Consult a physician prior to use in children under 10 years of age.

Warnings: Stop use and ask a doctor if symptoms persist or worsen. In case of overdose, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, take only on advice of physician.

Other Information: Store in a cool dry place. Tamper resistant for your protection. Use only if safety seal is intact.

Keep out of reach of children.

Uses

Indications: For temporary relief of hunger sensations, overeating, obesity, overweight, adipose storage, excessive appetite, cravings for sweets & starches, abdominal fat.

Active ingredient

Active Ingredient: Adrenalinum, Adrenocorticotrophin, Agrimonia eupatoria, flos, Anacardium orientale, Antimonium crudum, Calcarea carbonica, Castanea sativa, flos, Cortisone aceticum, Fucus vesiculosus, Hypothalamus, Kali bichromicum, Oleander, Pituitarum posterium, Sabadilla, Staphysagria, Thyroidinum. All in equal volumes of each ingredient in 10X, 30X and LM1 potencies.

Inactive ingredients: Citric acid, Demineralized water, Potassium sorbate.

Purpose

Indications

For temporary relief of:

  • hunger sensations
  • overeating
  • obesity
  • overweight
  • adipose storage
  • excessive appetite
  • cravings for sweets & starches
  • abdominal fat

Ultra Pure

Ultra Pure

Adrenalinum, Adrenocorticotrophin, Agrimonia eupatoria, flos, Anacardium orientale, Antimonium crudum, Calcarea carbonica, Castanea sativa, flos, Cortisone aceticum, Fucus vesiculosus, Hypothalamus, Kali bichromicum, Oleander, Pituitarum posterium, Sabadilla, Staphysagria, Thyroidinum LIQUID

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:55924-0002
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Epinephrine EPINEPHRINE 10 [hp_X]
Corticotropin CORTICOTROPIN 10 [hp_X]
AGRIMONIA EUPATORIA FLOWER AGRIMONIA EUPATORIA FLOWER 10 [hp_X]
SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE 10 [hp_X]
Antimony Trisulfide Antimony Trisulfide 10 [hp_X]
OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]
CASTANEA SATIVA FLOWER CASTANEA SATIVA FLOWER 10 [hp_X]
CORTISONE ACETATE CORTISONE 10 [hp_X]
FUCUS VESICULOSUS FUCUS VESICULOSUS 10 [hp_X]
BOS TAURUS HYPOTHALAMUS BOS TAURUS HYPOTHALAMUS 10 [hp_X]
POTASSIUM DICHROMATE DICHROMATE ION 10 [hp_X]
Nerium Oleander Leaf NERIUM OLEANDER LEAF 10 [hp_X]
SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND 10 [hp_X]
SCHOENOCAULON OFFICINALE SEED SCHOENOCAULON OFFICINALE SEED 10 [hp_X]
DELPHINIUM STAPHISAGRIA SEED DELPHINIUM STAPHISAGRIA SEED 10 [hp_X]
THYROID, UNSPECIFIED THYROID, UNSPECIFIED 10 [hp_X]

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
water
POTASSIUM SORBATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55924-0002-1 29.6 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-05-28


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Be sure to consult your doctor before taking any medication!
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