Label: FIRST AID ONLY STING RELIEF- benzocaine swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated April 10, 2018

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  • ACTIVE INGREDIENT

    Benzocaine 20 percent

    Menthol 1 percent

  • PURPOSE

    Topical Analgesic

    Topical Analgesic

  • INDICATIONS & USAGE

    Uses

    For temporary relief of the pain and itching of

    •insect bites and stings

    •minor scrapes and burns

  • WARNINGS

    Warnings

    For external use only.

    Do not use

    •in the eyes •if you are allergic to any of the ingredients

    Stop use and ask a doctor if •conditions worsen •symptoms clear up and then recur •the condition persists for more than 7 days

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children

    If swallowed, contact Poison Control 800.222.1222, or a doctor immediately.

  • DOSAGE & ADMINISTRATION

    Directions If stinger is present, remove carefully if possible.

    Adults Reverse cardboard sleeve so swab is visible. With cardboard sleeve on ampile, crush at dot on sleeve.

    There will be a "pop" and the swab will become saturated. Apply saturated applicator to the affected area no more than

    3 to 4 times daily.

    Children under 2 Consult a doctor.

  • INFORMATION FOR PATIENTS

    Other Information

    Store at room temperature.

  • INACTIVE INGREDIENT

    D&C Green no. 5, D&C yellow no.10, FD&C blue no.1, isopropyl alcohol, polyethylene glycol 300, purified water

  • QUESTIONS

    Questions 800.835.2263

  • PRINCIPAL DISPLAY PANEL

    Sting Swabs Carton ImageBOX19001-revD (002).jpg

  • INGREDIENTS AND APPEARANCE
    FIRST AID ONLY STING RELIEF 
    benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5250(NDC:46414-2040)
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.12 g  in 0.6 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.006 g  in 0.6 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-5250-0110 in 1 CARTON02/01/2010
    16 mL in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/01/2010
    Labeler - Acme United Corporation (001180207)
    Registrant - Acme United Corporation (001180207)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation045924339relabel(0924-5250) , repack(0924-5250)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation080119599relabel(0924-5250) , repack(0924-5250)
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