Label: NICOTINE STOP SMOKING AID- nicotine patch

  • NDC Code(s): 87278-008-01
  • Packager: Guangxi Keyun E-commerce Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 3, 2026

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  • ACTIVE INGREDIENT

    NICOTINE(7mg)

  • PURPOSE

    Stop Smoking Aid

  • INDICATIONS & USAGE

    Helps reducewithdrawal symptoms,such as nicotine cravings,during smoking cessation.

  • WARNINGS

    For external use only. flammable,keep away from heat or flame.

  • DO NOT USE

    Not for non-smokers.

  • WHEN USING

    When using section. Avoid smoking or using other nicotine-containing products to prevent nicotine overdose
    Consult doctor if pregnant/nursing

  • STOP USE

    OTC-Stop Use Section.If you experience severe skin irritation, rregular heartbeat, or: symptoms of nicotine overdose(e.g., dizziness, nausea, vomiting)

  • KEEP OUT OF REACH OF CHILDREN

    Keep away from children/pets.

  • DOSAGE & ADMINISTRATION


    Apply one patch to a clean, dry,and hairless area of skin(e.g.,upper arm or torso).
    Replace thepatchevery24hourswithanewone.
    Rotate application sites to avoid skin irritation.
    Step1+(28mg)-For smokers of 10+ cigarettes/day.
    Applyonupperarm/hip;avoidbrokenskin.
    Replaceafter24hours.

  • INACTIVE INGREDIENT

    2-Hydroxyethyl Acrylate
    Powdered Cellulose
    Methacrylic Acid

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    NICOTINE STOP SMOKING AID 
    nicotine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87278-008
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE7 mg
    Inactive Ingredients
    Ingredient NameStrength
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    2-HYDROXYETHYL ACRYLATE (UNII: 25GT92NY0C)  
    METHACRYLIC ACID (UNII: 1CS02G8656)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87278-008-0160 in 1 BOX03/20/2026
    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)03/20/2026
    Labeler - Guangxi Keyun E-commerce Co., Ltd. (517165491)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangxi Keyun E-commerce Co., Ltd.517165491manufacture(87278-008)
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