Label: 4% LIDOCAINE PAIN RELIEF PATCH- lidocaine 4% patch

  • NDC Code(s): 87278-003-01
  • Packager: Guangxi Keyun E-commerce Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 29, 2026

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

  • ACTIVE INGREDIENT

    Lidocaine 4%

  • PURPOSE

    Topical anesthetic

  • INDICATIONS & USAGE

    For temporary relief of pain

  • WARNINGS

    For external use only

  • DO NOT USE


    more than 1 patch at a time
    on wounds or damaged skin
    with a heating pad
    if you are allergic to any ingredients of this product

  • WHEN USING


    use only as directed
    avoid contact with the eyes,mucous membranes or rashes
    do not bandage tightly

  • STOP USE


    localized skin reactions occur,such as rash,itching,redness,irritation, pain,swelling and blistering
    condition worsen
    symptoms persist for more than 7 days
    symptoms clear up and occur again within a few days

  • KEEP OUT OF REACH OF CHILDREN


    If pregnant or breast-feeding, ask a health professional before use.
    Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION


    Adult and children 12 years of age and over:
    clean and dry affected area
    remove film from patch and apply to the skin (see illustration)
    apply 1 patch at a time to affected area, not more than 3 to 4 times daily
    remove patch from the skin after at most 8-hour application
    Children under 12 years of age: consult a doctor

  • INACTIVE INGREDIENT

    Glycerin
    Dihydroxyaluminum aminoacetate anhydrous
    Edetate disodium
    Tartaric acid
    Povidone K90
    DMDM Hydantoin
    Polysorbate 80
    Propylene glycol
    Carboxymethylcellulose sodium
    Kaolin
    Carbomer
    Sodium polyacrylate
    Water

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    4% LIDOCAINE PAIN RELIEF PATCH 
    lidocaine 4% patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87278-003
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE0.04 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    KAOLIN (UNII: 24H4NWX5CO)  
    DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)  
    CARBOMER (UNII: 0A5MM307FC)  
    TARTARIC ACID (UNII: W4888I119H)  
    POVIDONE K90 (UNII: RDH86HJV5Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87278-003-0130 in 1 BOX; Type 0: Not a Combination Product01/29/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/29/2026
    Labeler - Guangxi Keyun E-commerce Co., Ltd. (517165491)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangxi Keyun E-commerce Co., Ltd.517165491manufacture(87278-003)