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PROLONG

Medically reviewed on August 7, 2018

Dosage form: gel
Ingredients: BENZOCAINE 2833mg in 60mL
Labeler: Product Max Group Inc
NDC Code: 70742-089

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.

PROLONG - 089

Drug Facts
Active 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 under cap is broken or missing.

Inactive Ingredients

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

PROLONG product label

www.bodyactionproducts.com

Distributed by:

Body Action Products

Lutz, FL 33559

ACTION BODY PRODUCTS

Benzocaine Male Genital Desensitizer

PROLONG

FOR MEN

Helps Prolong Sexual Pleasure

Lubricating Gel

2 FL OZ (60 ml)

PROLONG 
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-089
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (BENZOCAINE) BENZOCAINE2833 mg  in 60 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) 
METHYLPARABEN 
POLYETHYLENE GLYCOL 400 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
Packaging
#Item CodePackage Description
1NDC:70742-089-0160 mL in 1 BOTTLE
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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