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PROLONG

Medically reviewed by Drugs.com. Last updated on Jul 28, 2021.

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

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.