Label: LIDOCAINE PAIN RELIEF ROLL-ON- lidocaine 4% liquid

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

Drug Label Information

Updated December 18, 2024

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  • DOSAGE & ADMINISTRATION

    Adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily.

    Children under 2 years of age: consult a doctor.

  • INACTIVE INGREDIENT

    acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexylglycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, methylparaben, polysorbate 60, SD alcohol 40 (15%), steareth-2, steareth-21, water

  • ACTIVE INGREDIENT

    Lidocaine 4%

  • WARNINGS

    For External Use Only.

    When using this product:

    use only as directed

    do not bandage tightly or use with a heating pad

    avoid contact with eyes

    do not apply to wounds or damaged skin

    do not use in large quantities

    partifcularly over raw surfaces or blistered areas

  • KEEP OUT OF REACH OF CHILDREN

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

  • INDICATIONS & USAGE

    For temporarily relief of pain and itching.

  • PURPOSE

    Topical analgesic

  • PRINCIPAL DISPLAY PANEL

    CVS Lidocaine LBLCVS Lidocaine IFCCVS Lidocaine CartonCVGSLido.jpglido

  • INGREDIENTS AND APPEARANCE
    LIDOCAINE PAIN RELIEF ROLL-ON 
    lidocaine 4% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-029
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    WATER (UNII: 059QF0KO0R)  
    STEARETH-21 (UNII: 53J3F32P58)  
    ALCOHOL (UNII: 3K9958V90M)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    CETETH-20 PHOSPHATE (UNII: 921FTA1500)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-029-971 in 1 CARTON06/05/2019
    174 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/05/2019
    Labeler - CVS Pharmacy (062312574)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(69842-029) , analysis(69842-029) , label(69842-029) , pack(69842-029)
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