Label: FIRST AID DIRECT SOOTHE-A-STING- benzocaine swab sponge

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

Drug Label Information

Updated December 28, 2023

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  • ACTIVE INGREDIENT

    Active Ingredients (each swab)

    Benzocaine (20%), L-Methanol (1%)

  • PURPOSE

    Purpose

    Analgesic

  • Uses

    For the temporary relief of pain and itching associated with insect bites and stings

  • Warnings

    FOR EXTERNAL USE ONLY

    • do not use in the eyes
    • not for prolonged use
  • Stop use and ask doctor

    if condition for this preparation is used persists, or if a rash or irritation develops.

  • Keep out of reach of children. 

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Reverse cardboard sleeve then crush at dot between thumb and forefinger. Once solution has saturated tip, apply to sting or bite.

  • Other Information

    Store at room temperature away from light.

  • Inactive Ingredients

    D&C Green Dye #5, D&C Yellow Dye #10, FD&C Blue Dye #1, PEG 300 NF, Isopropyl Alcohol, Purified Water, USP

  • Questions? 

    Call 1-908-362-9266 Monday through Friday, 9:00am - 5:00pm e.s.t

  • Principal Display Panel - Box

    10 SWABS

    (1/2 ml.)

    UNIT NO

    U1-19

    SOOTHE-A-STING-SWABS

    (FOR INSECT STINGS)

    ACTIVE INGREDIENTS: 

    BENZOCAINE 20%

    MENTHOL 1%

    DISTRIBUTED BY

    first aid direct®

    Mason, OH 45040

    Box

  • INGREDIENTS AND APPEARANCE
    FIRST AID DIRECT SOOTHE-A-STING 
    benzocaine swab sponge
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42961-107
    Route of Administrationtopical
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 mg  in 100 mg
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM1 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    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)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42961-107-0210 in 1 BOX05/16/2022
    10.5 mg in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/16/2022
    Labeler - Cintas Corporation (056481716)
    Establishment
    NameAddressID/FEIBusiness Operations
    JAMES ALEXANDER CORP040756421manufacture(42961-107)
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