Label: ENDLESS LOVE FOR MEN- benzocaine gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated August 7, 2016

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

  • Drug FactsActive Ingredient

    Benzocaine 5%

  • Purpose

    Male Genital Desensitizer

  • Keep out of reach of children

    Keep out of reach of children.

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

  • Uses

    Helps in the prevention of premature ejaculation.

  • Warnings

    For external use only.

    • Avoid contact with the eyes
    • 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.
    • If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor.
  • Directions

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

    Do not use if safety seal is broken or missing.

  • Inactive Ingredients

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

  • endless LOVEFOR MEN product label

    endless LOVE

    FOR MEN

    BY BODY ACTION

    STAY HARD & PROLONG
    BENZOCAINE MALE GENITAL DESENSITIZER

    1.7 FL OX (50 ml)

    Endless Love for Men Stay Hard & Prolong Water Based Lubricating Gel is a genital desensitizer that delays ejaculation and helps prolong sexual pleasure.

    www.BODYACTIONPRODUCTS.COM

    ACTION BODY PRODUCTS

    Distributer by:
    Body Action Products

    Lutz, FL 33559

    PMG End Love

  • INGREDIENTS AND APPEARANCE
    ENDLESS LOVE  FOR MEN
    benzocaine gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-072
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE2410 mg  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) (UNII: 8136Y38GY5)  
    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:70742-072-0150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/15/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34806/15/2016
    Labeler - Product Max Group Inc (134893911)
    Registrant - Product Max Group Inc (134893911)