Label: HIMS DELAY WIPES- benzocaine wipes dressing

  • NDC Code(s): 71730-009-03, 71730-009-12
  • Packager: Hims Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 7, 2023

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

View All Sections
  • Warnings

    For external use only

    When using this prouct avoid contact with the eyes


    Stop and ask doctor if: the 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. If symptoms persist.

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

  • 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 Ingredient

    Benzocaine 7% Male Genital Desensitizer

  • Inactive Ingredient

    Propylene glycol

  • Keep out of reach of children

    Keep out of reach of children

  • Quesitons?

    For questions or comments call 1-800-368-0038   

  • Other Information

    Made in the USA with US and imported materials.

    Distributed by HIMS, Inc., 2269 Chestnut Street #523, San Francisco, CA 94123

  • Labeling

    Hims Delay Wipes UC 12 Artwork

  • INGREDIENTS AND APPEARANCE
    HIMS DELAY WIPES 
    benzocaine wipes dressing
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71730-009
    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:71730-009-033 in 1 CARTON06/14/2021
    13 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:71730-009-1212 in 1 CARTON06/14/2021
    23 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/14/2021
    Labeler - Hims Inc. (080678637)
    Registrant - Swiss-American CDMO, LLC (080170933)
    Establishment
    NameAddressID/FEIBusiness Operations
    Swiss-American CDMO, LLC080170933manufacture(71730-009)
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!