Label: NATURES CRAFT LIDOCAINE MALE GENITAL DESENSITIZER- lidocaine hydrochloride liquid

  • NDC Code(s): 73382-185-01
  • Packager: Natures Design Products LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

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

View All Sections
  • DRUG FACTS:

  • Active Ingredient:

    Lidocaine HCl 10mg/Spray

    Male Genital Desensitizer

  • Indications:

    • For temporary male genital desensitization, helping to slow the onset of ejaculation.
  • Warnings:

    Avoid contact with eyes.

    Keep out of reach of children.

    • If swallowed, consult physician.
    • Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, discontinue use and consult a physician.
    • If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult physician.
  • 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.
  • Additional Information:

    Store at room temperature.

  • Other Ingredients:

    Aqua (Deionized Water), Ethylhexylglycerin, Isopropyl Myristate, Parfum (Fragrance), Phenoxyethanol, Polysorbate-20, Stearic Acid.

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    NATURES CRAFT LIDOCAINE MALE GENITAL DESENSITIZER 
    lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73382-185
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73382-185-011 in 1 BOX04/05/2021
    130 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 DrugM01704/05/2021
    Labeler - Natures Design Products LLC (032583117)
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!