Nicotine Transdermal System Step 3

Nicotine


Golden State Medical Supply, Inc.
Human Otc Drug
NDC 60429-443
Nicotine Transdermal System Step 3 also known as Nicotine is a human otc drug labeled by 'Golden State Medical Supply, Inc.'. National Drug Code (NDC) number for Nicotine Transdermal System Step 3 is 60429-443. This drug is available in dosage form of Patch, Extended Release. The names of the active, medicinal ingredients in Nicotine Transdermal System Step 3 drug includes Nicotine - 7 mg/24h . The currest status of Nicotine Transdermal System Step 3 drug is Active.

Drug Information:

Drug NDC: 60429-443
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Nicotine Transdermal System Step 3
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base: Nicotine
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix: transdermal system step 3
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Nicotine
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Golden State Medical Supply, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Patch, Extended Release
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:NICOTINE - 7 mg/24h
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TRANSDERMAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: NDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 12 Nov, 1999
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 15 Jan, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: NDA020076
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Golden State Medical Supply, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:198029
198030
198031
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
NUI:N0000175706
M0014836
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:6M3C89ZY6R
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:Cholinergic Nicotinic Agonist [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:Nicotine [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Cholinergic Nicotinic Agonist [EPC]
Nicotine [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
60429-443-1414 PATCH in 1 CARTON (60429-443-14) / 24 h in 1 PATCH23 Sep, 2015N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Purpose stop smoking aid

Product Elements:

Nicotine transdermal system step 1 nicotine methacrylic acid nicotine nicotine nicotine transdermal system step 2 nicotine methacrylic acid nicotine nicotine nicotine transdermal system step 3 nicotine methacrylic acid nicotine nicotine

Indications and Usage:

Use reduces withdrawal symptoms, including nicotine craving, associated with quitting smoking

Warnings:

Warnings section if you are pregnant or breast-feeding, only use this medicine on the advice of your health care provider. smoking can seriously harm your child. try to stop smoking without using any nicotine replacement medicine. this medicine is believed to be safer than smoking. however, the risks to your child from this medicine are not fully known. ask a doctor before use if you have •heart disease, recent heart attack, or irregular heartbeat. • nicotine can increase your heart rate.high blood pressure not controlled with medication. • nicotine can increase your blood pressure.an allergy to adhesive tape or have skin problems, because you are more likely to get rashes. • stomach ulcer or diabetes.history of seizures. ask a doctor or pharmacist before use if you are •using a non-nicotine stop smoking drug •taking a prescription medicine for depression or asthma. your prescription dose may need to be adjusted. when using this product •if you have vivid dreams or other sleep d
isturbances remove this patch at bedtime• stop use and ask a doctor if •skin redness caused by the patch does not go away after four days, or if your skin swells, or you get a rash •irregular heartbeat or palpitations occur. •you get symptoms of nicotine overdose, such as nausea, vomiting, dizziness, weakness and rapid heartbeat. •you have symptoms of an allergic reaction (such as difficulty breathing or rash). keep out of reach of children and pets •used patches have enough nicotine to poison children and pets. • if swallowed, get medical help or contact a poison control center right away. • save pouch to use for patch disposal. • dispose of the used patches by folding sticky ends together and putting in pouch.

When Using:

When using this product •if you have vivid dreams or other sleep disturbances remove this patch at bedtime•

Dosage and Administration:

Directions if you are under 18 years of age, ask a doctor before use before using this product, read the enclosed self-help guide for complete directions and other information begin using the patch on your quit day if you smoke more than 10 cigarettes per day, use the following schedule below: step 1 step 2 step 3 use one 21 mg patch/day use one 14 mg patch/day use one 7 mg patch/day weeks 1-4 weeks 5-6 weeks 7-8 if you smoke 10 or less cigarettes per day , start with step 2 for 6 weeks, then step 3 for 2 weeks apply one new patch every 24 hours on skin that is dry, clean and hairless remove backing from patch and immediately press onto skin. hold for 10 seconds. wash hands after applying or removing patch. save pouch to use for patch disposal. dispose of the used patches by folding sticky ends together and putting in pouch. the used patch should be removed and a new one applied to a different skin site at the same time each day if you have vivid dreams, you may remove the patch at bed
time and apply a new one in the morning do not wear more than one patch at a time do not cut patch in half or into smaller pieces do not leave patch on for more than 24 hours because it may irritate your skin and loses strength after 24 hours to avoid possible burns, remove patch before undergoing any mri (magnetic resonance imaging) procedures it is important to complete treatment. if you feel you need to use the patch for a longer period to keep from smoking, talk to your health care provider.

Stop Use:

Stop use and ask a doctor if •skin redness caused by the patch does not go away after four days, or if your skin swells, or you get a rash •irregular heartbeat or palpitations occur. •you get symptoms of nicotine overdose, such as nausea, vomiting, dizziness, weakness and rapid heartbeat. •you have symptoms of an allergic reaction (such as difficulty breathing or rash).

Package Label Principal Display Panel:

Principal display panel nicotine transdermal system patch 21 mg delivered over 24 hours stop smoking aid includes: behavior support program with self-help guide step 1 if you smoke more than 10 cigarettes per day: start with step 1 if you smoke 10 or less cigarettes per day: start with step 2 carton21mg.jpg

Principal display panel nicotine transdermal system patch 14 mg delivered over 24 hours stop smoking aid includes: behavior support program with self-help guide step 2 if you smoke more than 10 cigarettes per day: use after completing step 1 if you smoke 10 or less cigarettes per day: start with step 2 carton14mg.jpg

Principal display panel nicotine transdermal system patch 7 mg delivered over 24 hours stop smoking aid includes: behavior support program with self-help guide step 3 for use after completing step 2 carton7mg.jpg

Further Questions:

Questions or comments? call 1-800-585-8682 weekdays (9am-8pm et) or visit us at www.habitrol.com to increase your success in quitting: 1. you must be motivated to quit. 2. use one patch daily according to directions. 3. it is important to complete treatment. 4. if you feel you need to use the patch for a longer period to keep from smoking, talk to your health care provider. 5. use patch with a behavioural support program, such as the one described in the enclosed booklet. for your family's protection, patches are supplied in child-resistant pouches. do not use if individual pouch is open or torn. not for sale to persons under 18 years of age. proof of age required. not for sale in vending machines or from any source where proof of age cannot be verified.


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.