MINT RX ENDURANCE WIPES- benzocaine liquid 
PHARMAMEDRX

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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MINT RX ENDURANCE WIPES
BENZOCAINE USP 5%

Active ingredient

Benzocaine 5%

Purpose

Male genital desensitizer

Keep out of reach of children

If swallowed, get medical help or contact a poison control center right away

Use

Helps in temporarily prolonging time until ejaculation

Warnings

For external use ony

When using this product avoid contact with eyes

Stop use and ask a doctor if

This product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision

You or your partner develop a rash or irritation such as burning or itching

Symptoms persist

Directions

Wipe head and shaft of penis before intercourse or use as directed by a doctor.  Wash product off of penis after intercourse

Inactive ingredients

Purified water, ethyl alcohol, glycerin, Vitamin E, phenoxyethanol

MINT RX ENDURANCE WIPES
BENZOCAINE USP 5%

8 PACKET in 1 BOX > 2 mL in 1 PACKET

MINT RX ENDURANCE WIPES 
benzocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77691-433
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
TOCOPHEROL (UNII: R0ZB2556P8)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77691-433-088 in 1 PACKAGE05/20/2020
1NDC:77691-433-032 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34805/20/2020
Labeler - PHARMAMEDRX (063814205)
Registrant - PHARMAMEDRX (063814205)
Establishment
NameAddressID/FEIBusiness Operations
PHARMAMEDRX063814205manufacture(77691-433)

Revised: 5/2020
Document Id: 7c0865de-55c8-421c-8ea2-2d77ab1b73d3
Set id: 566910b7-3fa3-47d3-8d05-286fc1ce636f
Version: 1
Effective Time: 20200520
 
PHARMAMEDRX