Label: NERVIVE PAIN RELIEVING LIQUID ROLL-ON- lidocaine hcl and menthol liquid

  • NDC Code(s): 69423-970-03
  • Packager: The Procter & Gamble Manufacturing Company
  • 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.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Lidocaine HCl 4%

    Menthol 1%

    Active ingredients Purpose

    Topical anesthetic

    Topical analgesic

  • Use

    temporarily relieves minor pain

  • Warnings

    For external use only

    Flammable •
    keep away from heat and open flame

  • Do not use

    • If you have had an allergic reaction to lidocaine or other local anesthetics

    • on large areas of the body or on cut, irritated, blistered, or swollen skin

    • on puncture wounds

    • for more than one week without consulting a doctor

  • When using this product

    • use only as directed. Read and follow all directions and warnings on this carton.

    • avoid contact with eyes and mucous membranes

    • rare cases of serious burns have been reported with products of this type

    • do not apply to wounds or damaged, broken or irritated skin

    • do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use

    • a transient burning sensation may occur upon application but generally disappears in several days

    • avoid applying into skin folds

  • Stop use and ask a doctor if

    • condition worsens

    • severe burning sensation, redness, rash or irritation develops

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

    • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

  • If pregnant or breast-feeding,

    ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children and pets.

  • SPL UNCLASSIFIED SECTION

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    adults and children over 12 years:


    • apply a thin layer to affected area every 6 to 8 hours
    • do not exceed 3 applications in a 24 hour period
    • massage into painful area until thoroughly absorbed into skin
    AFTER APPLYING, WASH HANDS WITH SOAP AND WATER
    children 12 years or younger:ask a doctor

    Store at no greater than 25°C (77°F).

  • Inactive ingredients

    acrylates/C10-30 alkyl acrylate crosspolymer, alcohol, aminomethylpropanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl
    methicone, ceteth-20 phosphate, cetostearyl alcohol, dicetyl phosphate, dimethicone, edetate disodium, ethylhexylglycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, phenoxyethanol, polyoxyl 15
    hydroxystearate, polysorbate 60, sorbitan isostearate, steareth-21, tocopherol, water

  • Questions?

    1-855-446-4345

  • SPL UNCLASSIFIED SECTION

    DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202

    NerviveHealth.com

  • PRINCIPAL DISPLAY PANEL - 2.5 OZ

    NERVIVE™ PAIN RELIEVING LIQUID ROLL-ON

    LIDOCAINE HCl & MENTHOL

    TARGETS MULTIPLE NERVE PAIN RECEPTORS

    MAXIMUM STRENGTH

    MEDICATED ROLL-ON NET WT 2.5 OZ (70.9 g)

    Nervive Roll-on

  • INGREDIENTS AND APPEARANCE
    NERVIVE PAIN RELIEVING  LIQUID ROLL-ON
    lidocaine hcl and menthol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-970
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE0.04 g  in 1 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    STEARETH-21 (UNII: 53J3F32P58)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CETETH-20 PHOSPHATE (UNII: 921FTA1500)  
    DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ALCOHOL (UNII: 3K9958V90M)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    CAPRYLYL TRIMETHICONE (UNII: H6HK6E4EB1)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)  
    POLYOXYL 15 HYDROXYSTEARATE (UNII: 71YMM1X75O)  
    ALUMINUM DICETYL PHOSPHATE (UNII: WMV3R5DS7O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-970-0370.9 g in 1 CANISTER; Type 0: Not a Combination Product02/08/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/08/2022
    Labeler - The Procter & Gamble Manufacturing Company (004238200)