Label: DYNAMO DELAY- lidocaine spray

  • NDC Code(s): 69664-001-01
  • Packager: Momentum Management LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 13, 2024

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  • 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

  • INGREDIENTS AND APPEARANCE
    DYNAMO DELAY 
    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
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    ALCOHOL (UNII: 3K9958V90M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Packaging
    #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
    unapproved drug other05/13/2015
    Labeler - Momentum Management LLC (828734397)
    Registrant - Westwood Laboratories, LLC (832280635)
    Establishment
    NameAddressID/FEIBusiness Operations
    Westwood Laboratories, LLC832280635label(69664-001) , pack(69664-001) , manufacture(69664-001)
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