Label: MYCRATINE MIGRAINE RELIEF liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 42638-7666-2, 42638-7666-3 - Packager: Nico Worldwide, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 18, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PRINCIPAL DISPLAY PANEL
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
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.
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DOSAGE & ADMINISTRATION
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 INGREDIENT
- OTHER SAFETY INFORMATION
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INGREDIENTS AND APPEARANCE
MYCRATINE MIGRAINE RELIEF
mycratine migraine relief liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42638-7666 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 6 [hp_X] in 60 mL TYROSINE (UNII: 42HK56048U) (TYROSINE - UNII:42HK56048U) TYROSINE 30 mg in 60 mL PHENYLALANINE (UNII: 47E5O17Y3R) (PHENYLALANINE - UNII:47E5O17Y3R) PHENYLALANINE 20 mg in 60 mL TRYPTOPHAN (UNII: 8DUH1N11BX) (TRYPTOPHAN - UNII:8DUH1N11BX) TRYPTOPHAN 40 mg in 60 mL CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 85 mg in 60 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 59150 mg in 60 mL SUCRALOSE (UNII: 96K6UQ3ZD4) 10 mg in 60 mL SODIUM CITRATE (UNII: 1Q73Q2JULR) 45 mg in 60 mL SODIUM BENZOATE (UNII: OJ245FE5EU) 10 mg in 60 mL Product Characteristics Color white (Clear) Score Shape Size Flavor LEMON Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42638-7666-3 1 in 1 BOX 1 NDC:42638-7666-2 60 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/15/2013 Labeler - Nico Worldwide, Inc. (138642314) Registrant - Nico Worldwide, Inc. (138642314) Establishment Name Address ID/FEI Business Operations Nico Worldwide, Inc. 138642314 manufacture(42638-7666) , pack(42638-7666)
