Label: DYNAMO DELAY SAMPLE BOTTLE- lidocaine spray

  • NDC Code(s): 69664-003-02
  • 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 May 31, 2024

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  • ACTIVE INGREDIENT

    Lidocaine USP 13%
    (approximately 10 mg per spray)

  • PURPOSE

    Topical Anesthetic

  • USE(S)

    • 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

    Dynamo Delay
    NDC 69664-003-02
    Lidocaine USP 13%
    (approximately 10 mg per spray)
    Male Genital Desensitizer Spray
    Helps in temporarily prolonging the time until ejaculation.
    .088 fl oz (2.6mL)
    Made in the USA


    dd-sb-302-label

    dd-sb-302-box

  • INGREDIENTS AND APPEARANCE
    DYNAMO DELAY SAMPLE BOTTLE 
    lidocaine spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69664-003
    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:69664-003-021 in 1 BOX05/31/2024
    12.6 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED DRUG OTHER05/31/2024
    Labeler - Momentum Management LLC (828734397)
    Registrant - Westwood Laboratories, LLC (832280635)
    Establishment
    NameAddressID/FEIBusiness Operations
    Westwood Laboratories, LLC832280635LABEL(69664-003) , MANUFACTURE(69664-003) , PACK(69664-003)
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