Label: BITE AND STING RELIEF WIPE- alcohol 50% lidocaine hcl 2% cloth

  • Category: HUMAN OTC DRUG LABEL

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 July 5, 2019

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  • Active Ingredients

    Ethyl Alcohol 50.0%

    Lidocaine HCL 2.0%

  • Purpose

    First Aid Antiseptic
    Topical Analgesic

  • Uses

    • First aid to help guard against skin infection and temporary relief of pain and itching assocaiated with insect bites.
  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    Do not use

    • in the eyes over large areas of the body or bandage. 
    • in large quantities particularly over raw surfaces or blistered areas.
    Stop use and contact a doctor if the condition persists or worsens for more than 7 days or clears up and occurs again within a few days.
  • Keep out of reach of children 

    Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and children 2 years and older: Apply to clean affected area no more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

  • Inactive ingredients

    Benzalkonium Chloride, Menthol, Water.

  • Packaging

    Inner LabelOuter Box

  • INGREDIENTS AND APPEARANCE
    BITE AND STING RELIEF WIPE 
    alcohol 50% lidocaine hcl 2% cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-190
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL50 mL  in 100 mL
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    MENTHOL (UNII: L7T10EIP3A)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-190-1030 in 1 BOX06/01/2019
    13 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34806/01/2019
    Labeler - CVS (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Diamond Wipes International, Inc.161104729manufacture(69842-190)
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