Label: WALGREENS BURN- lidocaine hydrochloride gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 31, 2023

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

View All Sections
  • Active Ingredient

    Lidocaine HCl 4%

  • Purpose

    Topical analgesic

  • Uses

    Temporarily relieves pain and itching due to: minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations

  • Warnings

    For external use only

    Do Not Use

    In large quantities, particularly over raw surfaces or blistered areas

    When Using This Product

    Do not get into eyes

    Stop use and ask doctor if

    condition gets worse

    symptoms last 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.

  • Directions

    • adults and children 2 years and over: apply to affected area not more than 3 to 4 times daily

    • children under 2 years: ask a doctor
  • Other information

    Store between 20 °C and 25 °C (68 °F and 77 °F)

  • Inactive Ingredients

    Aloe barbadensis (aloe vera) leaf juice, caprylyl glycol, dimethyl isosorbide, glycerin, hydroxyethyl cellulose, phenoxyethanol, purified water, vitamin E

  • Principal Display Panel

    Package Label

  • INGREDIENTS AND APPEARANCE
    WALGREENS BURN 
    lidocaine hydrochloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-2020-251 in 1 CARTON07/16/2021
    174 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/16/2021
    Labeler - WALGREENS (008965063)
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!