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
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated April 23, 2021

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

  • 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/C 10-30 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
    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

    NET WT 3 OZ (85 g)

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

    CVS
    Health™

    MAXIMUM STRENGTH*

    Lidocaine
    Plus

    PAIN RELIEVING CREAM

    LIDOCAINE HCl 4%
    BENZYL ALCOHOL 10%

    Topical anesthetics

    Non-greasy

    • Fast acting
    • Numbing relief
    • Unscented

    NET WT 3 OZ (85 g)

    Principal-Display Panel – 85 g Tube 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 BOX04/23/2021
    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 not finalpart34804/23/2021
    Labeler - NATURAL ESSENTIALS, INC. (947484713)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURAL ESSENTIALS, INC.947484713MANUFACTURE(66902-758)