Label: POWERECT BENZOCAINE MALE DELAY GEL- benzocaine gel

  • NDC Code(s): 81923-367-00, 81923-367-01
  • Packager: SKINS SEXUAL HEALTH LIMITED
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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  • DRUG FACTS

  • ACTIVE INGREDIENT:

    Benzocaine 5.00%

    Purpose:

    Male genital desensitizer

  • USES:

    Helps to temporarily prevent premature ejaculation.

  • WARNINGS:

    Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, discontinue use and consult a physician. If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician.

    FOR EXTERNAL USE ONLY.Avoid contact with eyes.

    Keep out of reach of children.

    If product is swallowed, get medical attention or contact poison control center immediately.

  • DIRECTIONS:

    Apply product to the head and shaft of the penis prior to intercourse, or as directed by your physician. Wipe away excess product.

  • INACTIVE INGREDIENTS:

    Aqua (deionized Water), Ethylhexylglycerin, Hydroxyethylcellulose, l-Arginine, Lepidium Meyenii (Maca) Extract, Panax Ginseng Root Extract, PEG-8, Phenoxyethanol, Propylene Glycol.

  • OTHER INFORMATION:

    Store in a cool dry place below 30°C (86°F) out of direct sunlight.

  • QUESTIONS?

    Contact us on +44 1636 593943

  • Package Labeling:3ml

    Bottle5

  • Package Labeling:15ml

    Bottle6

  • INGREDIENTS AND APPEARANCE
    POWERECT BENZOCAINE MALE DELAY GEL 
    benzocaine gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81923-367
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    ARGININE (UNII: 94ZLA3W45F)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81923-367-003 mL in 1 PACKET; Type 0: Not a Combination Product10/03/2022
    2NDC:81923-367-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product10/03/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/03/2022
    Labeler - SKINS SEXUAL HEALTH LIMITED (221947744)
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