Label: KEEPS CLIMAX DELAY- lidocaine hydrochloride liquid

  • NDC Code(s): 52261-0801-1
  • Packager: Cosco International, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 17, 2024

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

  • Drug Facts

    Active Ingredient....................Purpose

    Lidocaine HCL 9.6%..................Male Genital Desensitizer

  • Uses

    For temporary male genital desensitization, helping to slow the onset of ejaculation.

  • Warnings

    For external use only.

    When using this product

    avoid contact with eyes.

  • Stop use and ask a doctor if

    • you or your partner develop a rash or irritation, such as burning or itching.
    • this product does not provide relief if used as directeed.  Premature ejaculation may be due to a condition requiring medical supervision.

    Keep out of reach of children.

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

    Directions

    Apply 3 or more sprays, not to exceed 10, to head and shaft of penis before intercourse, or use as directed by a doctor.  Wash product off after intercourse.

    Other information

    Store at room temperature 68°F to 77°F

    Inactive ingredients

    Alcohol, Benzyl Alcohol, Ethoxydiglycol, Isopropyl Myristate, Panthenol, Phenoxyethanol, Polysorbate 20, Tocopheryl Acetate, Water

  • PRINCIPAL DISPLAY PANEL

    bottle label

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    carton label

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  • INGREDIENTS AND APPEARANCE
    KEEPS CLIMAX DELAY 
    lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52261-0801
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.0096 kg  in 1 kg
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52261-0801-11 in 1 CARTON06/01/2024
    10.00052 kg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/01/2024
    Labeler - Cosco International, Inc. (016433141)
    Registrant - Cosco International, Inc. (016433141)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosco International, Inc.016433141manufacture(52261-0801) , label(52261-0801) , pack(52261-0801)