Label: STING RELIEF PAD- benzocaine, alcohol swab

  • 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 October 18, 2022

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  • Active Ingredient

    Active Ingredient: Purpose:

    Benzocaine, 6% w/v.................. Topical Anesthetic

    SD alcohol, 60% w/v.................. Antiseptic

  • Purpose


    Topical Anesthetic

    Antiseptic

  • Uses

    Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

  • Directions

    Clean intended area thoroughly with pad. Discard after single use.

  • Warnings

    Warnings: For external use only.

    Avoid contact with eyes. If this happens, rinse thoroughly with water.

  • Keep out of reach of children

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

  • Inactive Ingredients

    Purified water

  • STORAGE AND HANDLING

    Flammable - keep away from fire or flame.

  • DO NOT USE

    Do not use: In eyes, on broken skin, deep puncture wounds. If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.

  • Package labeling

    label

  • INGREDIENTS AND APPEARANCE
    STING RELIEF PAD 
    benzocaine, alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71584-0109
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 g  in 100 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71584-0109-10.5 mL in 1 PACKAGE; Type 0: Not a Combination Product06/14/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34806/14/2018
    Labeler - Guangdong Comfort Medical Products Co., Ltd. (544507534)
    Registrant - Guangdong Comfort Medical Products Co., Ltd. (544507534)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Comfort Medical Products Co., Ltd.544507534manufacture(71584-0109)
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