PREBOOST- benzocaine liquid 
944 Corp

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.

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Male Genital Desensitizer
Towelette

Drug Facts

Active Ingredients

Benzocaine USP 4.0%

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.

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 – pouch label

PREBOOST™

MALE DESENSITIZING WIPES

Helps in temporarily
prolonging time until ejaculation

Developed by Dr. Harry Fisch
www.preboost.com

1 single-use premoistened towelette

Manufactured for 944 Corp
944 Park Ave, New York, NY 10028 www.preboost.com

PRINCIPAL DISPLAY PANEL – pouch label

PRINCIPAL DISPLAY PANEL – box label

PREBOOST™

MALE DESENSITIZING WIPES

Helps in temporarily prolonging time until ejaculation

10 single-use
premoistened towelette

Developed by Dr. Harry Fisch
|www.preboost.com

PRINCIPAL DISPLAY PANEL – box label
PREBOOST 
benzocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62192-8500
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5) benzocaine4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
alcohol (UNII: 3K9958V90M)  
water (UNII: 059QF0KO0R)  
propylene glycol (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62192-8500-110 in 1 BOX
11.2 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34802/18/2014
Labeler - 944 Corp (054365072)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec of America, Inc.874965262MANUFACTURE(62192-8500)

Revised: 2/2014
Document Id: 40f108d6-4c4d-4adb-983a-486692eb7dbd
Set id: 5da84dea-e28e-474a-a33a-e72db27bffad
Version: 2
Effective Time: 20140218
 
944 Corp