Label: NERVIVE PAIN RELIEVING CREAM- lidocaine hcl and menthol cream

  • NDC Code(s): 84126-318-03
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 6, 2024

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Lidocaine HCl 4%

    Menthol 1%

    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 and pets.

    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

  • STORAGE AND HANDLING

    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

  • PRINCIPAL DISPLAY PANEL - 3.0 OZ

    NERVIVE™

    PAIN RELIEVING CREAM

    LIDOCAINE HCl & MENTHOL

    TARGETS MULTIPLE

    NERVE PAIN RECEPTORS

    PENETRATING CREAM

    MEDICATED CREAM NET WT 3.0 OZ (85.1 g)

    318

  • INGREDIENTS AND APPEARANCE
    NERVIVE PAIN RELIEVING  CREAM
    lidocaine hcl and menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-318
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)  
    POLYOXYL 15 HYDROXYSTEARATE (UNII: 71YMM1X75O)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
    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)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ALCOHOL (UNII: 3K9958V90M)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84126-318-031 in 1 CARTON08/12/2024
    185.1 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/12/2024
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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!