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Preboost by The Female Health Company d/b/a Veru Healthcare

Dosage form: liquid
Ingredients: benzocaine 4g in 100mL
Labeler: The Female Health Company d/b/a Veru Healthcare
NDC Code: 69681-432

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.

PREBOOST®

Drug Facts

Active Ingredient

Benzocaine USP 4%

Purpose

Male Genital Desensitizer

Use

Helps in temporarily prolonging time until ejaculation

Warnings

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 develops 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, or use as directed by a doctor. Wash product off after intercourse.

Inactives

Purified water, Ethyl Alcohol (SDA 40B), Propylene Glycol

PRINCIPAL DISPLAY PANEL - 10 Wipes Packet Box

Clinically Proven to Make Sex Last Longer

PREBOOST®
KEEP IT GOING

10 Single-Use Wipes
Male desensitizing wipes for
prolonging the time until ejaculation

H Fisch MD
Created by Dr. Harry Fisch, Named
"One of America's Best Doctors"

PREBOOST 
benzocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69681-432
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzocaine (benzocaine) benzocaine4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
alcohol 
water 
propylene glycol 
Packaging
#Item CodePackage Description
1NDC:69681-432-1010 PACKET in 1 BOX
11.2 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/30/2015
Labeler - The Female Health Company d/b/a Veru Healthcare (055300578)
Establishment
NameAddressID/FEIOperations
Safetec of America, Inc.874965262MANUFACTURE(69681-432)

 
The Female Health Company d/b/a Veru Healthcare

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Medically reviewed on Apr 7, 2017

Further information

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

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