Label: MINT RX ENDURANCE WIPES- benzocaine liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 20, 2020

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  • Active ingredient

    Benzocaine 5%

  • Purpose

    Male genital desensitizer

  • Keep out of reach of children

    If swallowed, get medical help or contact a poison control center right away

  • Use

    Helps in temporarily prolonging time until ejaculation

  • Warnings

    For external use ony

    When using this product avoid contact with eyes

  • Stop use and ask a doctor if

    This product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision

    You or your partner develop a rash or irritation such as burning or itching

    Symptoms persist

  • Directions

    Wipe head and shaft of penis before intercourse or use as directed by a doctor.  Wash product off of penis after intercourse

  • Inactive ingredients

    Purified water, ethyl alcohol, glycerin, Vitamin E, phenoxyethanol

  • MINT RX ENDURANCE WIPESBENZOCAINE USP 5%

    8 PACKET in 1 BOX > 2 mL in 1 PACKET

  • INGREDIENTS AND APPEARANCE
    MINT RX ENDURANCE WIPES 
    benzocaine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77691-433
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77691-433-088 in 1 PACKAGE05/20/2020
    1NDC:77691-433-032 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34805/20/2020
    Labeler - PHARMAMEDRX (063814205)
    Registrant - PHARMAMEDRX (063814205)
    Establishment
    NameAddressID/FEIBusiness Operations
    PHARMAMEDRX063814205manufacture(77691-433)
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