Label: DZEUS CLIMAX CONTROL WIPES- benzocaine cloth

  • NDC Code(s): 54723-006-01
  • Packager: Sambria Pharmaceuticals, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 17, 2024

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

View All Sections
  • Drug Facts

  • Active ingredient

    Benzocaine USP 7%

  • Purpose

    Male genital desensitizer

  • Uses

    • Aids in the prevention of premature ejaculation
    • Aids in temporarily prolonging the time until ejaculation
  • Warnings

    For External Use only.
    Do not use onbroken or inflamed skin.
    If pregnant or breastfeeding, ask a health professional before use.
    When using thisproduct, avoid contact with eyes.
    Stop and ask doctor if:
    This product, when used as directed, does not provide relief; premature ejaculation may be due to a condition requiring medical supervision,you or your partner develop rash or irritation, such as burning or itching  symptoms persist.

  • Keep out of reach of children 

    In case of ingestion, seek professional assistance and contact poison control immediately.

  • Directions

    Use wipe to apply a small amount of product to the head and shape of the penis before intercourse, or as directed by a doctor. Wash off after intercourse.
    Allow product to dry prior to intercourse.
    Not suitable for oral use.
    Use as directed.

  • Other information

    Store between 20°-25 °C (68°-77 °F)

  • Inactive ingredients

    Lactic Acid, Phenol, Phenoxyethanol, ethylhexylglycerin, Polyethylene Glycol, purified water

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    DZEUS CLIMAX CONTROL WIPES 
    benzocaine cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE7 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    PHENOL (UNII: 339NCG44TV)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54723-006-013 mL in 1 POUCH; Type 0: Not a Combination Product12/08/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/08/2021
    Labeler - Sambria Pharmaceuticals, LLC (078676259)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!