Label: STING RELIEF SWAB- benzocaine swab

  • NDC Code(s): 82749-010-01
  • Packager: Epic Medical Supply Corp
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated October 29, 2024

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  • SPL UNCLASSIFIED SECTION

  • Active Ingredients (each swab)

    Benzocaine USP (20%), L-Menthol USP (1%)

  • Purpose

    analgesic

  • Uses

    For 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
    • do not apply other medications to the same affected areas unless advised by a doctor

    Stop use and ask a doctor if condition for this preparation is used persists, or if a rash, irritation or allergic reaction develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. Not for use with children less than 2 years old without medical advice. If swallowed, get medical help immediately 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 topically to the sting or bite. May be used on affected area(s) up to 4 times per day.

  • 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 USP, Purified Water USP.

  • Packaging

    Package

  • INGREDIENTS AND APPEARANCE
    STING RELIEF SWAB 
    benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82749-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM0.006 g  in 0.6 mL
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.12 g  in 0.6 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82749-010-016 mL in 1 CARTON; Type 0: Not a Combination Product10/29/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/29/2024
    Labeler - Epic Medical Supply Corp (101423894)
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