Label: DYNAMO DELAY- lidocaine spray

  • NDC Code(s): 69664-001-01
  • Packager: Momentum Management LLC
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 17, 2022

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

  • Active Ingredient

    Lidocaine USP 13%

    (approximately 10 mg per spray)

  • Purpose

    Topical Anesthetic

  • Uses

    • for temporary male genital desensitization, helping to slow the onset of ejaculation
    • helps in temporarily prolonging the time until ejaculation
    • for reducing oversensitivity in the male in advance of intercourse
  • Warnings

    For external use only

  • When using this product

    avoid contact with the eyes

  • Stop use and ask a doctor if:

    • this 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.
  • Keep out of reach of children

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

  • 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
  • Inactive Ingredients

    Isopropyl Palmitate, SD Alcohol 40B, Stearic Acid

  • Questions?

    310 446 1632 Monday - Friday 9am-5pm(PST)

    Manufactured for

    Momentum Management LLC

    1206 W Jon St

    Torrance, CA 90502

  • Principal Display Panel

    Screaming O

    Dynamo Delay

    NDC 69664-001-01

    Lidocaine USP 13%

    (appromixately 10 mg per spray)

    Male Genital Desensitizer Spray

    Helps in temporarily prolonging the time until ejaculation

    3/4 fl oz (22.2mL)

    Made in the USA

    Outer Box

    Bottle Label:

    Bottle Label

    lidocaine spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69664-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE10 mg  in 0.08 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69664-001-011 in 1 BOX05/13/2015
    122.2 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34805/13/2015
    Labeler - Momentum Management LLC (828734397)
    NameAddressID/FEIBusiness Operations
    Westwood Laboratories Inc832280635manufacture(69664-001)