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Magic STAMINA

Medically reviewed by Drugs.com. Last updated on Jun 25, 2018.

Dosage form: liquid
Ingredients: BENZOCAINE 1417mg in 30mL
Labeler: Product Max Group Inc
NDC Code: 70742-088

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.

Magic STAMINA - 088

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 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

MAGIC STAMINA 
benzocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-088
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (BENZOCAINE) BENZOCAINE1417 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
METHYLPARABEN 
POLYETHYLENE GLYCOL 400 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
Packaging
#Item CodePackage Description
1NDC:70742-088-0130 mL in 1 PACKAGE
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)

 
Product Max Group Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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