Label: NICOTINE TRANSDERMAL SYSTEM- nicotine patch, extended release
- NDC Code(s): 11673-194-01, 11673-194-02, 11673-195-02, 11673-196-02
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated March 21, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient Step 1 (in each patch)
- Active ingredient Step 2 (in each patch)
- Active ingredient Step 3 (in each patch)
- Purpose
- Use
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Warnings
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
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 disturbances remove this patch at bedtime
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Directions
- if you are under 18 years of age, ask a doctor before use
- before using this product, read the enclosed User’s 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 according to the following 10 week schedule:
STEP 1
STEP 2
STEP 3
Use one 21mg patch/day
Use one 14mg patch/day
Use one 7mg patch/day
Weeks 1-6
Weeks 7-8
Weeks 9-10
- if you smoke 10 or less cigarettes per day,do not use STEP 1 (21mg).Start with STEP 2 (14mg)for 6 weeks, then STEP 3 (7mg)for 2 weeks and then stop.
- steps 2 and 3 allow you to gradually reduce your level of nicotine. Completing the full program will increase your chances of quitting successfully.
- apply one new patch every 24 hours on skin that is dry, clean and hairless. Save pouch for disposing of the patch after use.
- remove backing from patch and immediately press onto skin. Hold for 10 seconds.
- wash hands after applying or removing patch. Throw away the patch by folding sticky ends together. Replace in its pouch and discard. See enclosed User’s Guide for safety and handling.
- you may wear the patch for 16 or 24 hours.
- if you crave cigarettes when you wake up, wear the patch for 24 hours.
- if you have vivid dreams or other sleep disturbances, you may remove the patch at bedtime and apply a new one in the morning
- the used patch should be removed and a new one applied to a different skin site at the same time each day
- 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
- it is important to complete treatment. If you fell you need to use the patch for a longer period to keep from smoking, talk to your health care provider.
- Other information
- Inactive ingredients
-
Questions or comments?
call toll-free 1-888-367-7919
(English/Spanish) weekdays
Includes User’s Guide with behavioral support program enrollment offer.
To increase your success in quitting:
- You must be motivated to quit.
- Complete the full treatment program, applying a new patch every day.
- Use with a support program as described in the enclosed User’s Guide.
- Not for sale to those 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.
For your family's protection, nicotine patches are supplied in child-resistant pouches. Do not use if individual pouch/packet is damaged or open.
Read carton and enclosed User's Guide before using this product. Keep the carton and User's Guide. They contain important information
100% satisfaction guaranteed or your money back.
094 09 0437 R00ID255400
Distributed by Target Corporation
Minneapolis, MN 55403
Shop Target.com
*NICODERM and CQ are registered trademarks owned by and/or licensed to the GSK group of companies.
What is the nicotine patch and how is it used?
The nicotine patch is a small, nicotine-containing patch. When you put on a nicotine patch, nicotine passes through the skin and into your body. The nicotine patch is very thin and uses special material to control how fast nicotine passes through the skin. Unlike the sudden jolts of nicotine delivered by cigarettes, the amount of nicotine you receive remains relatively smooth throughout the 24 or 16 hour period you wear the nicotine patch. This helps to reduce cravings you may have for nicotine.
READ THE LABEL
-
Principal Display Panel
NDC 11673-194-02
nicotine patch
nicotine transdermal system
21mg delivered over 24 hours
stop smoking aid
up & up ™
14PATCHES
Compare tothe active ingredient in NicoDerm ®CQ ®*
If you smoke more than 10 cigarettesper day, start with step 1
If you smoke 10 or less cigarettesper day, start with step 2
STEP 1
14 CLEAR PATCHES (2-WEEK KIT)
ACTUAL SIZE
© 2015 Target Brands, Inc.
30768XC
-
Principal Display Panel
NDC 11673-195-02
nicotine patch
nicotine transdermal system
14mg delivered over 24 hours
stop smoking aid
up & up ™
14PATCHES
Compare tothe active ingredient in NicoDerm ®CQ ®*
If you smoke 10 or less cigarettesper day, start with step 2
If you smoke more than 10 cigarettesper day, start with step 1
STEP 2
14 CLEAR PATCHES (2-WEEK KIT)
ACTUAL SIZE
© 2015 Target Brands, Inc.
30769XC
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
NICOTINE TRANSDERMAL SYSTEM
nicotine patch, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-194 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 21 mg in 24 h Inactive Ingredients Ingredient Name Strength HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) ETHYLENE-VINYL ACETATE COPOLYMER (40% VINYL ACETATE) (UNII: L5F16ZG4ZU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-194-02 14 in 1 CARTON 02/16/2000 1 24 h in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) 2 NDC:11673-194-01 7 in 1 CARTON 02/16/2000 2 24 h in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020165 02/16/2000 NICOTINE TRANSDERMAL SYSTEM
nicotine patch, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-195 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 14 mg in 24 h Inactive Ingredients Ingredient Name Strength HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) ETHYLENE-VINYL ACETATE COPOLYMER (40% VINYL ACETATE) (UNII: L5F16ZG4ZU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-195-02 14 in 1 CARTON 02/16/2000 1 24 h in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020165 02/16/2000 NICOTINE TRANSDERMAL SYSTEM
nicotine patch, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-196 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 7 mg in 24 h Inactive Ingredients Ingredient Name Strength HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) ETHYLENE-VINYL ACETATE COPOLYMER (40% VINYL ACETATE) (UNII: L5F16ZG4ZU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-196-02 14 in 1 CARTON 02/16/2000 1 24 h in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020165 02/16/2000 Labeler - Target Corporation (006961700) Registrant - Haleon US Holdings LLC (079944263)