Label: EQUATE PAIN RELIEF CREAM- 4% lidocaine hcl liquid

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

Drug Label Information

Updated December 19, 2023

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  • DOSAGE & ADMINISTRATION

    Adults and children 2 yrs 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.

  • 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, particularly over raw surfaces or blistered areas.

  • INACTIVE INGREDIENT

    actylates/C10-C30 Alkyl Acrylate Crosspolymer

    Aloe Barbadensis Leaf Etract

    Aminoethyl Propanol

    C30-C40 Alkyl Cetearyl Dimethicone Crosspolymer

    Caprylyl Methicone

    Cetearyl Alcohol

    Ceteth-20 Phosphate

    Dicetyl Phosphate

    Dimethicone

    Disodium EDTA

    Ethylhexylglycerin

    Glyceryl Stearate

    Methylparaben

    SD Alcohol 40

    Steareth021

    Purified water

  • INDICATIONS & USAGE

    For temporary relief of pain and itching.

  • KEEP OUT OF REACH OF CHILDREN

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

  • PURPOSE

    Topical Analgesic

  • ACTIVE INGREDIENT

    Lidocaine 4%

  • PRINCIPAL DISPLAY PANEL

    lidocaine

  • INGREDIENTS AND APPEARANCE
    EQUATE PAIN RELIEF CREAM 
    4% lidocaine hcl liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-634
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    STEARETH-21 (UNII: 53J3F32P58)  
    WATER (UNII: 059QF0KO0R)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    DISODIUM HEDTA (UNII: KME849MC7A)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    CETEARYL PHOSPHATE (UNII: 4O6GCK4CTJ)  
    CETETH-20 PHOSPHATE (UNII: 921FTA1500)  
    (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)  
    C30-45 ALKYL METHICONE (UNII: NFX970DSI2)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-634-9774 mL in 1 CONTAINER; Type 0: Not a Combination Product12/21/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/21/2018
    Labeler - Walmart, Inc (051957769)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114label(49035-634) , pack(49035-634) , manufacture(49035-634) , analysis(49035-634)
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