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

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Mycratine

Nico Worldwide, Inc.
Nico Worldwide, Inc.




FULL PRESCRIBING INFORMATION

Mycratine Label Description

Mycratine

Active ingredient

Ingredients

  • Nicotinum (6x)

In a base of: Caffeine, L-Tyrosine, L-Tryptophan, L-Phenylalanine

Purpose

Mycratine Migraine Relief

Advanced Relief Formula

Liquid Shot

Keep out of reach of children.

Uses

Indications:

For the relief/treatment of migraines and headaches

Intended for adult use only

Warning:

Do not use if pregnant or breast-feeding or have pheylketonuria.

Consult your doctor or health care professional before use if you are taking prescription medication for depression such as MAO inhibitors or have asthma, high blood pressure, stomach ulcers, diabetes, or hyperthyroidism.

This product contains nicotine, a chemical known to the state of California to cause birth defects or other reproductive harm.

Caution:

  • For any suspected or known illness or dysfunction, always consult your physician or medical adviser first.
  • Do not use if seal is broken.
  • Discard any unused portion after 24 hours.
  • Store in a cool, dry place (50-90 F). Avoid excessive heat and extreme cold.

Directions:

  • Shake well.
  • Drink one bottle at first indication of migraine. Wait 5 to 15 minutes.  Migraine symptoms should decrease significantly and allow you to return to your normal activities.
  • In extreme migraine cases it may be necessary to take a second bottle 15 minutes after the first bottle. 
  • Recommended dosage not to exceed four bottles a day.
  • Refrigerate after opening.

Inactive Ingredients:

purified water, gum acacia, lemon oil, brominated vegetable oil, ester gum, citric acid, sodium benzoate, sucralose.

Questions or comments:  info@nicoworldwide.com

Homeopathic Complex Formula

Patent Pending

NDC 42638-7666-2

Mycratine

Mycratine Migraine Relief LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42638-7666
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
nicotine NICOTINE 6 [hp_X]
TYROSINE TYROSINE 30 mg
PHENYLALANINE PHENYLALANINE 20 mg
TRYPTOPHAN TRYPTOPHAN 40 mg
CAFFEINE 85 mg

Inactive Ingredients

Ingredient Name Strength
water
Sucralose
SODIUM CITRATE
SODIUM BENZOATE

Product Characteristics

Color
white (Clear)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42638-7666-2 60 in 1 BOTTLE
2 NDC:42638-7666-3 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-06-15


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Be sure to consult your doctor before taking any medication!
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