Label: SOOTHE-A-STING- alcohol, benzocaine cloth

  • 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 May 21, 2021

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Drug Facts
    Active Ingredients

    Ethyl alcohol 50.0%

    Benzocaine 2.0%

  • PURPOSE

    Purpose

    Ethyl alcohol .......... Antiseptic

    Benzocaine ........... Topical pain relief

  • INDICATIONS & USAGE

    Uses   temporary relief of pain and itching caused by insect bites and stings.

  • WARNINGS

    Warnings

    For external use only. Flammable. Keep away from fire or flame.

  • DO NOT USE

    Do not use ■ in large quantities, particularly over

    raw or blistered areas ■ near eyes, if this happens

    winse thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if condition worsens or

    persists for more than 7 days or clears up and returns

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get
    medical help or contact a Poison Control Center
    right away.

  • DOSAGE & ADMINISTRATION

    Directions ■spread an even layer of Sing Relief

    over affected area not mor than 3 to 4 times daily
    ■ for children under 2 years of age consult a physician

  • INACTIVE INGREDIENT

    Inactive ingredients purified water

  • Product Label

    aramark : The First Choice In First Aid

    SOOTHE-A-STING™

    WIPE

    NDC # 81238-0315-1

    1 premoistened towelette

    Manufactured for Aramark

    aramark        Lenexa, KS 66219

                         913-269-9611

    LOT

    0315 Soothe

    res

  • INGREDIENTS AND APPEARANCE
    SOOTHE-A-STING 
    alcohol, benzocaine cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81238-0315
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.50 mL  in 1 mL
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81238-0315-13 mL in 1 PACKET; Type 0: Not a Combination Product04/09/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34804/09/2021
    Labeler - Western First Aid Safety dba Aramark (043861524)
    Registrant - Western First Aid Safety dba Aramark (043861524)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lights Medical Manufacture Co., Ltd.529128649manufacture(81238-0315)