Label: CVS HEALTH LIDOCAINE PLUS PAIN RELIEVING- lidocaine hydrochloride, benzyl alcohol cream

  • NDC Code(s): 66902-758-03
  • Packager: NATURAL ESSENTIALS, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 1, 2024

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  • Active ingredients

    Benzyl alcohol 10%

    Lidocaine HCl 4%

  • Purpose

    Topical anesthetic

    Topical anesthetic

  • Use

    For the temporary relief of pain

  • Warnings

    For external use only

    Do not use

    • on wounds or damaged skin
    • in large quantities
    • with a heating pad
    • if you are allergic to any ingredients of this product

    When using this product

    • use only as directed
    • avoid contact with the eyes, mucous membranes or rashes
    • do not bandage tightly

    Stop use and ask a doctor if

    • skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering
    • conditions worsen
    • symptoms persist for more than 7 days
    • symptoms clear up and occur again within a few days

    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 12 years of age and over:
    • clean and dry affected area
    • apply to affected area not more than 3 to 4 times daily

    children 12 years or younger:ask a doctor

  • Other information

    • Avoid storing product in direct sunlight
    • Protect product from excessive moisture
    • Store with lid closed tightly
  • Inactive ingredients

    Acrylates/C10-30 Acrylate Crosspolymer, Aloe Vera Gel 10 X, Aminomethyl Propanol, Cetearyl Alcohol, Ceteth-20 Phosphate, Dicetyl Phosphate, Citric Acid, Deionized Water, Dimethicone, Hydroxyethyl Acrlyate/Sodium, Acryloyldimethyl Taurate Copolymer, Squalane, Polysorbate 60, Propylene Gylcol, SDA 40-B Alcohol, Steareth-21.

  • Principal-Display Panel – 85 g Carton Label

    CVS
    Health™

    Compare to the
    active ingredients in
    Salonpas ®Lidocaine
    PLUS Cream*

    MAXIMUM STRENGTH
    Lidocaine concentration
    without a prescription     ✝

    Lidocaine
    Plus

    PAIN RELIEVING CREAM

    LIDOCAINE HCl 4%

    BENZYL ALCOHOL 10%

    Topical anesthetics

    Non-greasy

    • Fast acting
    • Numbing relief
    • Unscented

    Non-greasy
    cream

    Package Contains
    One Tube

    ✝Among over the counter
    topical analgesics.

    NET WT 3 0Z (85 g)

    Principal-Display Panel – 85 g Carton Label
  • Principal-Display Panel – 85 g Carton Label

    CVS
    Health™

    MAXIMUM STRENGTH
    Lidocaine concentration
    without a prescription     ✝

    Lidocaine
    Plus

    PAIN RELIEVING CREAM

    LIDOCAINE HCl 4%

    BENZYL ALCOHOL 10%

    Topical anesthetics

    Non-greasy

    • Fast acting
    • Numbing relief
    • Unscented

    NET WT 3 0Z (85 g)

    Principal-Display Panel – 85 g Carton Label
  • INGREDIENTS AND APPEARANCE
    CVS HEALTH LIDOCAINE PLUS  PAIN RELIEVING
    lidocaine hydrochloride, benzyl alcohol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-758
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1 g
    BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETETH-20 PHOSPHATE (UNII: 921FTA1500)  
    DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    SQUALENE (UNII: 7QWM220FJH)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALCOHOL (UNII: 3K9958V90M)  
    STEARETH-21 (UNII: 53J3F32P58)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66902-758-031 in 1 BOX04/23/202112/31/2027
    185 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/23/202112/31/2027
    Labeler - NATURAL ESSENTIALS, INC. (947484713)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURAL ESSENTIALS, INC.947484713manufacture(66902-758)
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