MINT RX ENDURANCE WIPES- benzocaine liquid

MINT RX ENDURANCE WIPES by

Drug Labeling and Warnings

MINT RX ENDURANCE WIPES by is a Otc medication manufactured, distributed, or labeled by PHARMAMEDRX. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 WIPESBENZOCAINE USP 5%

INGREDIENTS AND APPEARANCE

MINT RX ENDURANCE WIPES 
benzocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77691-433
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHEROL (UNII: R0ZB2556P8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77691-433-08	8 in 1 PACKAGE	05/20/2020
1	NDC: 77691-433-03	2 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	05/20/2020

Labeler - PHARMAMEDRX (063814205)

Registrant - PHARMAMEDRX (063814205)

Establishment
Name	Address	ID/FEI	Business Operations
PHARMAMEDRX		063814205	manufacture(77691-433)