Label: LIDOCAINE DRY- lidocaine spray

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

Drug Label Information

Updated December 16, 2024

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

  • Active Ingredient

    Lidocaine 4%

  • Topical Anesthetic

  • Use

    temporarily relieves minor pain

  • Warnings

    For external use only

  • Do not use

    • On large areas of the body or on cut, irritated or swollen skin.
    • On puncture wounds
    • for more than one week without consulting a doctor
  • When using this product

    • Use only as directed. Read and follow all directions and warnings on this label
    • do not allow contact with the eyes and mucous membranes
    • avoid spraying on face
    • avoid inhalation of spray
    • do not bandage or apply local heatl(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 as a doctor if

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

    • do not use near heat or flame or while smoking
    • avoid long term storage above 104°F (40°C)
    • do not puncture or incinerate. Contents under pressure.
    • do not store at temperatures above 120°F (49°C)
  • 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 over 12 years:

    • spray affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
    • product will dry quickly on its own, and does not need to be rubbed in

    children 12 years or younger: ask a doctor

  • Inactive Ingredients

    caprylic/capric triglyceride, isobutane, propylene glycol, alcohol 40B (30%)

  • Principal Display Panel

    label

  • INGREDIENTS AND APPEARANCE
    LIDOCAINE DRY 
    lidocaine spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-543
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-543-04113 mL in 1 CAN; Type 0: Not a Combination Product07/22/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/22/2021
    Labeler - CVS (062312574)