DZEUS CLIMAX CONTROL WIPES- benzocaine cloth 
Sambria Pharmaceuticals, LLC

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Drug Facts

Active ingredient

Benzocaine USP 7%

Purpose

Male genital desensitizer

Uses

Warnings

For External Use only.
Do not use onbroken or inflamed skin.
If pregnant or breastfeeding, ask a health professional before use.
When using thisproduct, avoid contact with eyes.
Stop and ask doctor if:
This product, when used as directed, does not provide relief; premature ejaculation may be due to a condition requiring medical supervision,you or your partner develop rash or irritation, such as burning or itching  symptoms persist.

Keep out of reach of children 

In case of ingestion, seek professional assistance and contact poison control immediately.

Directions

Use wipe to apply a small amount of product to the head and shape of the penis before intercourse, or as directed by a doctor. Wash off after intercourse.
Allow product to dry prior to intercourse.
Not suitable for oral use.
Use as directed.

Other information

Store between 20°-25 °C (68°-77 °F)

Inactive ingredients

Lactic Acid, Phenol, Phenoxyethanol, ethylhexylglycerin, Polyethylene Glycol, purified water

Product label

image description

DZEUS CLIMAX CONTROL WIPES 
benzocaine cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE7 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
PHENOL (UNII: 339NCG44TV)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54723-006-013 mL in 1 POUCH; Type 0: Not a Combination Product12/08/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/08/2021
Labeler - Sambria Pharmaceuticals, LLC (078676259)

Revised: 1/2024
Document Id: 0f25f62a-c7db-ebf5-e063-6294a90a0e7b
Set id: 95caab25-c0c8-4b46-b3ce-7a1dd02a3dd2
Version: 5
Effective Time: 20240117
 
Sambria Pharmaceuticals, LLC