Label: BODY ACTION PRODUCTS HIGHER CONTROL MALE CLIMAX- benzocaine gel

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

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active Ingredient

    Benzocaine 5%

    Purpose

    Male Genital Desensitizer

  • 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.

    Keep out of reach of children.

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

  • 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 on bottle is broken or missing.

  • Inactive Ingredients

    Cannabis Sativa (Hemp) Seed Oil, Hydroxyethylcellulose, Methylparaben, PEG-8, Polysorbate 20, Propylene Glycol, Propylparaben, Water.

  • Package Labeling: BODY ACTION PRODUCTS: Higher Control Male Climax Gel, 2oz/60ml (70742-292-00)

    Label

  • INGREDIENTS AND APPEARANCE
    BODY ACTION PRODUCTS HIGHER CONTROL MALE CLIMAX 
    benzocaine gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-292
    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
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70742-292-0060 mL in 1 BOTTLE; Type 0: Not a Combination Product04/29/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/29/2022
    Labeler - PRODUCT MAX GROUP INC (134893911)
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