Label: EQUATE MAXIMUM STRENGTH PAIN RELIEVING 4% LIDOCAINE WITH LAVENDER ESSENTIAL OIL TOPICAL ANALGESIC- lidocaine hydrochloride liquid

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

Drug Label Information

Updated December 21, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Lidocaine HCl 4%

  • Purpose

    Topical analgesic

  • Use

    for the temporary relief of pain.

  • Warnings

    For external use only.

    When using this product

    • Avoid contact with the eyes.
    • Use only as directed. Read and follow all directions and warnings on this carton
    • Do not apply over large areas of the body.
    • Do not use on puncture wounds.
    • Do not bandage or apply local heat (such as heating pads) to the area of use or use with a medicated patch.
    • Do not allow contact with mucous membranes.
    • Do not use in large quantities, particularly over raw surfaces or blistered areas.
    • Do not use at the same time as other topical analgesics.

    Stop use and ask a doctor if

    • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
    • redness is present
    • irritation develops.

    Flammable

    • keep away from fire or flame.

    If pregnant or breast feeding ask a health professional before use.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

  • Directions

    Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: Do not use, consult a doctor.

  • Other information

    store at room temperature.

  • Inactive ingredients

    acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat., 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, fragrance, glyceryl stearate, isohexadecane, lavandula angustifolia (lavender) oil, phenoxyethanol, polysorbate 60, steareth-21, water.

  • Questions or comments?

    1-888-287-1915

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY: Walmart Inc.,
    Bentonville, AR 72716

  • PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton

    NDC 79903-229-01

    equate™

    Compare to
    Aspercreme®
    active
    ingredient*

    MAXIMUM STRENGTH

    Pain Relieving
    Liquid
    4% Lidocaine
    with Lavender
    Essential Oil

    No-Mess Applicator

    • Fast acting
    • Easy to apply
      to affected area

    2.5 FL OZ
    (73mL)

    PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton
  • INGREDIENTS AND APPEARANCE
    EQUATE MAXIMUM STRENGTH PAIN RELIEVING 4% LIDOCAINE WITH LAVENDER ESSENTIAL OIL   TOPICAL ANALGESIC
    lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-229
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    C30-45 Alkyl Cetearyl Dimethicone Crosspolymer (UNII: 4ZK9VP326R)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    Ceteth-20 Phosphate (UNII: 921FTA1500)  
    DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Ethylhexylglycerin (UNII: 147D247K3P)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    Isohexadecane (UNII: 918X1OUF1E)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Polysorbate 60 (UNII: CAL22UVI4M)  
    Steareth-21 (UNII: 53J3F32P58)  
    Water (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-229-011 in 1 CARTON12/05/2023
    173 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 drugM01712/05/2023
    Labeler - Walmart Inc. (051957769)
    Registrant - Garcoa, Inc. (036464697)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sigan Industries INC255106239MANUFACTURE(79903-229) , LABEL(79903-229) , PACK(79903-229)
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