NDC 42638-7664 Nicfix Plus

NDC Product Code 42638-7664

NDC 42638-7664-2

Package Description: 60000 mg in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Nicfix Plus with NDC 42638-7664 is product labeled by Nico Worldwide, Inc.. The product's dosage form is and is administered via form.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nico Worldwide, Inc.
Labeler Code: 42638
Start Marketing Date: 01-09-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Nicfix Plus Product Label Images

Nicfix Plus Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Ingredients: SNRA (Nicotinum 6X)In a base of: buffered caffeine anhydrous, L-tyrosine, L-phenylalanine

Otc - Purpose

Concentrated Liquid ShotNicFix+For when you CAN'T SMOKE... or CHOOSE not to.Minty Mojito2 fl. oz. (59 mL)

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDRENSuggested Use: 18 years of age or older

Indications & Usage

REFRIGERATE AFTER OPENINGIndications: Use when smoking is not allowed or when you should not smoke.Recommended for morning and early afternoon use.


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

SAFE TO USE WHILE SMOKINGDirections: Use as required. Do not use nicotine cessation products while using this product. Homeopathic Nicotinum Complex. Registeres as a homeopathic remedy.www.getyournicfix.com

Inactive Ingredient

Inactive Ingredients: purified water, natural flavors, liquid sucrose, citric acid, xanthan gum, luo han guo concentrate

Other Safety Information

ONCE OPENED USE WITHIN 48 HOURSPatented process NDC 42638-7685-2Distributed by Nico Worldwide, Inc.NicFix is a product of Nico Worldwide, Inc.320 Irving Dr., Oxnard, CA 93030www.nicoworldwide.com

* Please review the disclaimer below.