Label: NICFIX PLUS- nicotine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 42638-7664-2 - 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 January 27, 2014
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Warning: do not use if you are prenant or lactating or have phenylketonuria. Consult your doctor or health care professional before us if you are taking prescription medication for depression such as MAO inhibitors or have asthma, high blood pressure, stomach ulcers, diabetes, or hyperthyroidism. Nicotine or caffeine can increase your heart rate. This product contains nicotine, a chemical known to the state of California to cause birth defects or other reproductive harms.
Caution: For any suspected or known illness or dysfunction, always consult your physician or medical adviser first.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NICFIX PLUS
nicotine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42638-7664 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 3 mg in 60000 mg TYROSINE (UNII: 42HK56048U) (TYROSINE - UNII:42HK56048U) TYROSINE 30 mg in 60000 mg PHENYLALANINE (UNII: 47E5O17Y3R) (PHENYLALANINE - UNII:47E5O17Y3R) PHENYLALANINE 30 mg in 60000 mg CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 75 mg in 60000 mg CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID 45 mg in 60000 mg Inactive Ingredients Ingredient Name Strength SUCRALOSE (UNII: 96K6UQ3ZD4) 10 mg in 60000 mg SODIUM BENZOATE (UNII: OJ245FE5EU) 10 mg in 60000 mg WATER (UNII: 059QF0KO0R) 59760 mg in 60000 mg XANTHAN GUM (UNII: TTV12P4NEE) 10 mg in 60000 mg SIRAITIA GROSVENORII FRUIT (UNII: NOU2FB51TW) 10 mg in 60000 mg Product Characteristics Color Score Shape Size Flavor LIME, MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42638-7664-2 60000 mg in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/09/2014 Labeler - Nico Worldwide, Inc. (138642314) Establishment Name Address ID/FEI Business Operations Nico Worldwide, Inc. 138642314 manufacture(42638-7664)
