NDC 42638-7664

NicFix Plus

Nicotine

NicFix Plus is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Nico Worldwide, Inc.. The primary component is Nicotine; Tyrosine; Phenylalanine; Caffeine; Citric Acid Monohydrate.

Product ID42638-7664_620e053b-22c4-422b-b16a-3093e0601f6e
NDC42638-7664
Product TypeHuman Otc Drug
Proprietary NameNicFix Plus
Generic NameNicotine
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2014-01-09
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNico Worldwide, Inc.
Substance NameNICOTINE; TYROSINE; PHENYLALANINE; CAFFEINE; CITRIC ACID MONOHYDRATE
Active Ingredient Strength3 mg/60000mg; mg/60000mg; mg/60000mg; mg/60000mg; mg/60000mg
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 42638-7664-2

60000 mg in 1 BOTTLE (42638-7664-2)
Marketing Start Date2014-01-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 42638-7664-2 [42638766402]

NicFix Plus LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-09
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
NICOTINE3 mg/60000mg

OpenFDA Data

SPL SET ID:05d5761b-738f-46fa-833c-97901d1164de
Manufacturer
UNII

NDC Crossover Matching brand name "NicFix Plus" or generic name "Nicotine"

NDCBrand NameGeneric Name
42638-7664NicFix PlusNicFix Plus
0067-6011Meijer NICOTINE TRANSDERMAL SYSTEMNICOTINE
0067-6012Meijer NICOTINE TRANSDERMAL SYSTEMNICOTINE
0067-6013Meijer NICOTINE TRANSDERMAL SYSTEMNICOTINE
0135-0194NICODERMnicotine
0135-0195NICODERMnicotine
0135-0196NICODERMnicotine
0363-0451NicotineNicotine
0363-0455NicotineNicotine
0363-0457NicotineNicotine
0536-1106NICOTINENICOTINE
0536-1107NICOTINENICOTINE
0536-1108NICOTINENICOTINE
0536-5894NicotineNicotine
0536-5895NicotineNicotine
0536-5896NicotineNicotine
11673-194NICOTINEnicotine
0220-3657NicotinumNICOTINE
0009-5400Nicotrolnicotine
0009-5401Nicotrolnicotine

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