Label: NICOTINE PATCH- nicotine patch

  • NDC Code(s): 87704-002-01, 87704-003-01, 87704-004-01
  • Packager: Guangzhou Yunzhen Trading Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 19, 2026

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    NICOTINE 7mg
    NICOTINE 14mg
    NICOTINE 21mg

  • PURPOSE

    quit smoking

  • WARNINGS


    If pregnant or breastfeeding, use only on advice of healthcare provider.
    Smoking seriously harms your child. Try to quit without nicotine replacement if possible. This medicine is believed safer than smoking, but risks to your child are not fully known.

  • INDICATIONS & USAGE

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

  • DO NOT USE


    If pregnant or breastfeeding, use only on advice of healthcare provider.
    Smoking seriously harms your child. Try to quit without nicotine replacement if possible. This medicine is believed safer than smoking, but risks to your child are not fully known.

  • WHEN USING


    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 disturbances, remove the patch at bedtime

  • STOP USE

    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 beartbeat.
    you have symptoms of an allergic reaction (suchas difficulty breathing or rash).

  • KEEP OUT OF REACH OF CHILDREN

    Used patches contain enough nicotine to poison children or pets. If swallowed, get medical help or contact Poison Control immediately. Dispose by folding sticky ends together and placing in pouch.

  • DOSAGE & ADMINISTRATION

    If you are under 18 years of age, ask a doctor beforeuse

    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

    Weeks 1 thru 4 STEP 1:use one 21 mg patch/day

    Weeks 5 and 6 STEP 2:use one 14 mg patch/day

    Weeks 7 and 8 STEP 3:use one 7 mg patch/day

    · If you smoke <10 cigarettes/day: start with Step 2 for 6 weeks, then Step 3 for 2 weeks.·

    Under 18: ask a doctor before use.·

    Apply one new patch every 24 hours to dry, clean,hairless skin.

    Remove backing, press onto skin for 10 seconds.

    Wash hands after handling. Dispose of used patches by folding sticky ends together and placing in original pouch.

    Remove old patch and apply new one to a different skin site at the same time each day.

    If vivid dreams occur, remove patch at bedtime and apply new one in the morning

    Do not cut patch. Do not wear more than one patchat a time.·

    Do not leave on longer than 24 hours (may irritateskin and loses strength).

    Remove patch before MRI procedures to avoid burns.·

    Complete treatment. If you need to use longer to stay smoke-free, talk to your healthcare provider.

  • INACTIVE INGREDIENT

    Acrylate adhesive
    Aluminized polyester
    Cellulose paper
    Methacrylic acid copolymer

  • PRINCIPAL DISPLAY PANEL

    label2

  • PRINCIPAL DISPLAY PANEL

    label3

  • PRINCIPAL DISPLAY PANEL

    label4

  • INGREDIENTS AND APPEARANCE
    NICOTINE PATCH 
    nicotine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87704-002
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE7 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)  
    METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
    POLYESTER (ADIPIC ACID, 1,6-HEXANEDIOL, NEOPENTYL GLYCOL) (UNII: 571593769G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87704-002-0130 in 1 BOX05/20/2026
    110 in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/20/2026
    NICOTINE PATCH 
    nicotine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87704-003
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE14 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)  
    METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
    POLYESTER (ADIPIC ACID, 1,6-HEXANEDIOL, NEOPENTYL GLYCOL) (UNII: 571593769G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87704-003-0130 in 1 BOX05/20/2026
    11 in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/20/2026
    NICOTINE PATCH 
    nicotine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87704-004
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE21 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)  
    METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
    POLYESTER (ADIPIC ACID, 1,6-HEXANEDIOL, NEOPENTYL GLYCOL) (UNII: 571593769G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87704-004-0130 in 1 BOX05/20/2026
    11 in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/20/2026
    Labeler - Guangzhou Yunzhen Trading Co., Ltd. (451601414)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yunzhen Trading Co., Ltd.451601414manufacture(87704-002, 87704-003, 87704-004)