Label: PROMESCENT DELAY WIPES- benzocaine dressing

  • NDC Code(s): 55636-000-01, 55636-000-50
  • Packager: Absorption
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 20, 2024

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  • Warnings

    Avoid contact with the eyes.

    Premature ejaculation may be due to a condition requiring medical supervision. If this product, used as directed, does not provide relief, discontinue use and consult a doctor.


    If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor.

  • Directions

    Apply a small amount to head and shaft of penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.

  • Indications

    For reducing oversensitivity in the male in advance of intercourse.

  • Indications

    For reducing oversensitivity in the male in advance of intercourse.

  • Active Ingredients

    Benzocaine 7% Male Genital Desensitizer

  • Inactive Ingredient

    Propylene glycol

  • Questions?

    Visit Promescent.com

  • Keep out of reach of children

    Keep out of reach of children

  • Other Information

    Distributed by: Absorption Pharmaceuticals LLC, Las Vegas, NV 89118, USA. Phone 1-877-852-0106 for reporting serious adverse events associated with use of this product, or visit promescent.com

  • Labeling

    Delay Wipes UC 15 Artwork

  • INGREDIENTS AND APPEARANCE
    PROMESCENT DELAY WIPES 
    benzocaine dressing
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55636-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE70 g  in 1000 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55636-000-505 in 1 CARTON06/09/2021
    13 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:55636-000-013 g in 1 POUCH; Type 0: Not a Combination Product04/12/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/09/2021
    Labeler - Absorption (014937753)
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