Label: ENDLESS LOVE FOR MEN- benzocaine gel

  • NDC Code(s): 70742-360-50
  • Packager: Body Action Products, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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

View All Sections
  • Drug Facts

  • Active Ingredient

    Benzocaine 5%

    Purpose

    Male Genital Desensitizer

  • Uses

    • Helps in the prevention of premature ejaculation.
  • Warnings

    For extenal use only.

    • Avoid contact with the eyes.
    • Premature ejaculation may be due to a condition requiring medial supervision. If this product, used as directed, does not provide relief, discontinue use and consult a doctor.

    Keep out of reach of children.

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

  • Directions

    • Apply a small amount to head and shaft of penis before intercouse.
    • Wash product off after intercourse.
  • Other Information

    Do not use if safery seal is broken or missing.

  • Inactive Ingredients

    Hydroxyethylcellulose, Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water.

  • Package Labeling:

    Label6

  • INGREDIENTS AND APPEARANCE
    ENDLESS LOVE FOR MEN 
    benzocaine gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-360
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70742-360-5050 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/18/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/18/2017
    Labeler - Body Action Products, Inc (134893911)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source, LLC080354456manufacture(70742-360)
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!