Label: AID AND FIRST STING RELIEF PREP PAD- benzocaine 6%, sd alcohol 60% swab

  • NDC Code(s): 69139-203-01
  • Packager: YIWU HAODING MEDICAL CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 9, 2024

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  • Drug Facts

  • Active ingredient

    Benzocaine 6% w/v

    SD alcohol 60% w/v

  • Purpose

    Antibacterial

  • Uses

    Apply topically as needed to cleanse intended area.

    Discard after single use.

  • Warnings

    For external use only.

    Flammable, keep away for fire or flame.

    Do not use

    • In large quantities
    • Over large areas of the body
    • In eyes

    Stop use and ask a doctor if conditions worsen or persist.

    Stop use and ask a doctor if

    • the conditions persist or worsen
  • 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 of age and older use on hands and face to clean and refresh, allow skin to air dry

    For children under 2 years ask a doctor before use.

    Tear open packet, unfold towelltte and use to clean desired skin area, discard towelltte appropriately after use.

  • Inactive ingredients

    purified water

  • Sting Relief

    Mf StingRelief Wipes Label

  • INGREDIENTS AND APPEARANCE
    AID AND FIRST STING RELIEF PREP PAD 
    benzocaine 6%, sd alcohol 60% swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69139-203
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 g  in 100 g
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL60 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69139-203-011 in 1 PACKAGE01/09/2024
    10.3 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/09/2024
    Labeler - YIWU HAODING MEDICAL CO.,LTD (421362384)
    Establishment
    NameAddressID/FEIBusiness Operations
    YIWU HAODING MEDICAL CO.,LTD421362384manufacture(69139-203)
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