Label: CVS HEALTH SUNBURN RELIEF COOLING LIDOCAINE 0.5 PAIN-RELIEVING- lidocaine hcl gel

  • NDC Code(s): 51316-022-15, 51316-022-20
  • Packager: CVS Pharmacy
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 17, 2024

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  • Active ingredients

    Lidocaine 0.5% (as Lidocaine HCl)

  • Purpose

    External Analgesic

  • Uses

    For the temporary relief of pain and itching associated with sunburn, minor burns, 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 eyes.. If contact occurs, rinse with water to remove.
  • Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days
    • symptomes clear up and occur again within a few days.
  • Keep out of reach of children.

    • If swallowed, seek medical help or contact a Poison Control Center immediately.
  • Directions

    • Adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily.
    • Children under 2 years of age: ask a doctor.
  • Other information

    May stain some fabrics.

  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Benzophenone-4, Benzyl Alcohol, Blue 1, Carbomer, Isoceteth-20, Phenoxyethanol, Tetrasodium EDTA, Triethanolamine.

  • Label

    CVS38499A

  • INGREDIENTS AND APPEARANCE
    CVS HEALTH SUNBURN RELIEF COOLING LIDOCAINE 0.5 PAIN-RELIEVING 
    lidocaine hcl gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-022
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ISOCETETH-20 (UNII: O020065R7Z)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51316-022-15170 g in 1 BOTTLE; Type 0: Not a Combination Product10/05/2018
    2NDC:51316-022-20567 g in 1 BOTTLE; Type 0: Not a Combination Product10/05/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/05/2018
    Labeler - CVS Pharmacy (062312574)
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