Label: CVS MAXIMUM STRENGTH LIDOCAINE PLUS- benzyl alcohol, lidocaine hydrochloride spray

  • 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 December 1, 2022

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

  • Active ingredients

    Benzyl alcohol  10%

    Lidocaine HCl  4%

  • Purpose

    Topical anesthetic

  • Uses

    For temporary relief of pain

  • Warnings

    For external use only

    Flammable:

    Keep away from fire or flame

    -Do not use near heat or flame or while smoking.

    -avoid long term storage above 40 degree Celcius.

    -do not puncture or incinerate. COntents under pressure

    -do not store at temperatures above 49 degree Celcius

    Do not use

    • on large areas of the body or cut or wounds or damaged skin
    • on puncture wounds
    • for more than one week without consulting a doctor

    When using this product

    • use only as directed
    • avoid contact with the eyes, mucous membranes or rashes
    • avoid spraying on face
    • avoid inhalation of spray
    • do not bandage or apply local heat such as heating pads or a medicated patch to area of use
    • do not use at the same time as other topical analgesics

    Stop use and ask a doctor if

    • skin reactions occur, such as rash, itching, redness, irritaion, 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.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and children 12 years of age and over:

    • spray to affected area not more than 3 to 4 times daily

    Children under 12 years of age:

    consult a doctor

  • Other information

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

    alcohol denatured, arnica montana flower extract, calendula officinalis flower extract, camellia sinensis leaf extract, chamomilla recutita (matricaria) flower extract , dimethyl sulfone (msm), Echinacea angustifolia extract, ilex paraguariensis leaf extract, isopropyl myristate, juniperus communis fruit extract, purified water 

  • Questions or comments?

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  • Principal Display Panel

    Lido

  • INGREDIENTS AND APPEARANCE
    CVS MAXIMUM STRENGTH LIDOCAINE PLUS 
    benzyl alcohol, lidocaine hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-573
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL10 g  in 100 g
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CHAMOMILE (UNII: FGL3685T2X)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    JUNIPER BERRY (UNII: O84B5194RL)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-573-631 in 1 BOX05/15/2020
    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 finalpart34805/15/2020
    Labeler - CVS Pharmacy Inc. (062312574)