Label: 4% LIDOCAINE PATCHES- 4% lidocaine patch

  • NDC Code(s): 87394-002-01
  • Packager: Shenzhen Huayuan Hengsheng Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 14, 2026

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

View All Sections
  • ACTIVE INGREDIENT

    Lidocaine 4%

  • PURPOSE

    Topical analgesic

  • 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 have ever had an allergic reaction to this product or any of its ingredients

  • 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
    conditions worsen
    symptoms persist for more than 7 days
    symptoms clear up and occur again within a few days

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Adults 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 hours of application

    Children under 12 years of age: consult a doctor

  • INACTIVE INGREDIENT

    Aluminum Glycinate
    Disodium EDTA
    Ethylhexylglycerin
    Glycerin
    Phenoxyethanol
    Polyvinyl pyrrolidone
    Polysorbate 80
    Sodium carboxymethyl cellulose
    Sodium polyacrylate
    Sorbitol
    Tartaric Acid
    Titanium Dioxide
    Water

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    4% LIDOCAINE PATCHES 
    4% lidocaine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87394-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PVP (UNII: FZ989GH94E)  
    TARTARIC ACID (UNII: W4888I119H)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ALUMINUM GLYCINATE (UNII: 1K713C615K)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87394-002-0140 in 1 BOX04/13/2026
    11 in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/13/2026
    Labeler - Shenzhen Huayuan Hengsheng Technology Co., Ltd. (570254468)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Huayuan Hengsheng Technology Co., Ltd.570254468manufacture(87394-002)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!