Label: EVERLIT SURVIVAL STING RELIEF PAD- sting relief cloth

  • NDC Code(s): 72766-017-01
  • Packager: Yangzhou Suxiang Medical Instrument Co., Ltd.
  • 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 September 29, 2023

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  • ACTIVE INGREDIENT

    Benocaine 6% lsopropyl Alcohol 70%

  • PURPOSE

    Topical analgesic

    antiseptic

  • USES

    For prevention of infection in minor scrapes andtemporary relief of itching insect bites

  • WARNINGS

    For external use only.
    Flammable, keep away from fire or flame.

  • DO NOT USE

    with electrocautery procedures.
    In the eyes. If contact occurs, flush eyes with water.

  • STOP USE

    Stop Use lf irritation and redness develop. If condition continues,consult your health care practitioner.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed,get medical help or contacta Poison Control Center right away.

  • Directions

    Apply to affected area 3 or 4 times daily.
    For adults and children 2 years of age and older.

    Children under 2 years:consult physician.

  • other Information

    store at room temperature 15° - 30° C (59° - 86° F)

  • INACTIVE INGREDIENT

    purified water

  • Everlit Sting Relief Pad

    Sting Relief Pad

  • INGREDIENTS AND APPEARANCE
    EVERLIT SURVIVAL STING RELIEF PAD 
    sting relief cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72766-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.34 g
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL8 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72766-017-011 in 1 PACKET; Type 0: Not a Combination Product09/29/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/29/2023
    Labeler - Yangzhou Suxiang Medical Instrument Co., Ltd. (543387280)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yangzhou Suxiang Medical Instrument Co., Ltd.543387280manufacture(72766-017) , label(72766-017) , pack(72766-017)
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