Label: MAGIC STAMINA- benzocaine liquid

  • 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 June 24, 2016

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

View All Sections
  • Drug FactsActive Ingredient

    Benzocaine 5%

  • Purpose

    Male Genital Desensitizer

  • Uses

    Helps in the prevention of premature ejaculation.

  • Warnings

    For external use only.

    • Avoid contact with 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 tab is broken or missing.

  • Inactive Ingredients

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

  • Magic STAMINA product label

    Benzocaine Male genital Desensitizer

    Magic STAMINA®

    Climax contral spray

    1.0 FL. OZ. (30 mL)

    Distributed By: Body Action Products, Lutz FL 33559

    www.bodyactionproducts.com

    PMG STAMINA

  • INGREDIENTS AND APPEARANCE
    MAGIC STAMINA 
    benzocaine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-088
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE1417 mg  in 30 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:70742-088-0130 mL in 1 PACKAGE; 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)
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!