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KY Duration for Men

Medically reviewed by Drugs.com. Last updated on Aug 18, 2021.

Dosage form: gel
Ingredients: Benzocaine 7g in 100mL
Labeler: RB Health (US) LLC
NDC Code: 63824-259

KY® Duration® Gel for Men

Drug Facts

Active ingredient

Benzocaine USP 7%

Purpose

Male Genital Desensitizer

Uses
  • helps in the prevention of premature ejaculation
  • helps in temporarily prolonging the time until ejaculation

Warnings

For external use only

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.

Avoid contact with the eyes

If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor.

If pregnant or breastfeeding, ask a health professional before use

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 the head and shaft of the penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.
  • use only on intact, non-inflamed skin
  • allow gel to dry prior to intercourse
  • not suitable for oral use
  • use as directed, not more than four times per day

Other information
  • store between 20-25°C (68-77°F)
  • compatible with latex condoms
  • child resistent closure. Instructions for opening are included in the leaflet.
  • read the enclosed leaflet to achieve best results

Inactive Ingredients

carbomer homopolymer type B, polyethylene glycol

Questions?

1-800-756-5488

Dist. by: RB Health (US)
Parsippany, NJ 07054-0224

Made in China

PRINCIPAL DISPLAY PANEL - 5 mL Can Carton Label

NEW SMOOTH GEL

KY®
DURATION®
GEL FOR MEN

Male Genital Desensitizer
Benzocaine USP 7%

LAST LONGER
ENJOY THE MOMENT

COMPATIBLE WITH
LATEX CONDOMS

36 PUMPS
0.16 FL. OZ. (5.0 mL)

KY DURATION FOR MEN 
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-259
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzocaine (Benzocaine) Benzocaine7 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED) 
POLYETHYLENE GLYCOL, UNSPECIFIED 
Packaging
#Item CodePackage Description
1NDC:63824-259-011 CAN in 1 CARTON
15 mL in 1 CAN
2NDC:63824-259-042 POUCH in 1 CARTON
2NDC:63824-259-020.5 mL in 1 POUCH
3NDC:63824-259-051 POUCH in 1 PACKET
3NDC:63824-259-030.5 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34803/19/2018
Labeler - RB Health (US) LLC (081049410)

 
RB Health (US) LLC

Further information

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