Label: ALOE VERA GEL- lidocaine hcl, menthol gel

  • NDC Code(s): 56062-747-43
  • Packager: Publix Super Markets, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 2026

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  • Active ingredient

    Lidocaine HCl 0.7%

    Menthol 0.2%

  • Purpose

    Topical analgesic

  • Uses

    for the temporary relief of pain and itching associated with

    • 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

    avoid contact with the eyes

  • Stop use and ask a doctor if

    condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

  • 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 of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • Inactive ingredients

    water, alcohol denat., polysorbate 20, glycerin, Aloe barbadensis leaf juice, carbomer, benzophenone-4, sodium hydroxide, benzyl alcohol, phenoxyethanol, blue 1

  • ADVERSE REACTION

    DISTRIBUTED BY PUBLIX SUPER MARKETS, INC.,

    3300 PUBLIX CORPORATE PARKWAY,

    LAKELAND, FL 33811   1-888-267-3037

    publix.com

    PUBLIX GUARANTEE: COMPLETE SATISFACTION OR YOUR MONEY BACK

    SCAN HERE FOR MORE INFORMATION

    DSP-TN-21091

    DSP-MP-20087

  • principal display panel

    Relieving

    AFTER-SUN GEL

    TOPICAL ANALGESIC

    WITH ALOE

    WITH LIDOCAINE HCL AND MENTHOL.

    SUNBURN RELIEF.

    P

    16 FL OZ (1 PT) 473 mL

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    ALOE VERA GEL 
    lidocaine hcl, menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56062-747
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS7 mg  in 1 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56062-747-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/10/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/10/2017
    Labeler - Publix Super Markets, Inc. (006922009)
    Registrant - Nice-Pak Products, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, LLC119091514manufacture(56062-747)
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