Label: SWISS NAVY ENDURANCE RX- lidocaine spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 19, 2023

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  • Drug Facts

  • Active Ingredients (per spray)

    Lidocaine approx. 10mg

    Purpose

    Anesthetic

  • Use:

    Helps in temporarily slowing the onset of ejaculation.

  • WARNINGS:

    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. 

    • For topical use only.

    Do not use 

    • if you or your partner are allergic to Lidocaine or topical anesthetics.
    • Keep away from fire and flame.
    • Discontinue use if you or your partner develop a rash or irritation, such as burning or itching.
    • If symptoms persist, consult a doctor.
    • Do not spray on broken, irritated or sensitive skin.
    • Avoid contact with eyes.
    • For external use only.

    Keep out of reach of children.

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

  • DIRECTIONS:

    Apply 3 or more sprays, not to exceed to 10, to head and shaft of penis, 10 minutes before intercourse, or use as directed by a doctor

    Rub into the skin and immediately wash off any residue.

    Wash product off after intercourse.

  • INACTIVE INGREDIENTS:

    Deionized Water, Alcohol Denat., Glycerin, Aloe Barbadensis Leaf Juice Powder.

  • Packgae Labeling:

    Outer PackageInner Package

  • INGREDIENTS AND APPEARANCE
    SWISS NAVY ENDURANCE RX 
    lidocaine spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69872-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69872-003-151 in 1 BOX08/01/2017
    115 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/01/2017
    Labeler - PACKAGE SOLUTIONS LLC (054705875)
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