MAGIC STAMINA CLIMAX CONTROL (BENZOCAINE) LIQUID [PRODUCT MAX GROUP INC]

MAGIC STAMINA CLIMAX CONTROL (BENZOCAINE) LIQUID [PRODUCT MAX GROUP INC]
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NDC 70742-182-01
Set ID 1be9b77d-2633-4786-9396-aa48c1a8c44b
Category HUMAN OTC DRUG LABEL
Packager Product Max Group Inc
Generic Name
Product Class
Product Number
Application Number PART348
  • 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 is broken or missing.

  • Inactive Ingredients

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

  • Package Labeling:

    Label3

  • INGREDIENTS AND APPEARANCE
    MAGIC STAMINA CLIMAX CONTROL 
    benzocaine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-182
    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:70742-182-0130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34803/01/2018
    Labeler - Product Max Group Inc (134893911)

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