DZEUS CLIMAX CONTROL WIPES- benzocaine cloth

DZEUS Climax control wipes by

Drug Labeling and Warnings

DZEUS Climax control wipes by is a Otc medication manufactured, distributed, or labeled by Sambria Pharmaceuticals, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzocaine USP 7%

Purpose

Male genital desensitizer

Uses

• Aids in the prevention of premature ejaculation
• Aids in temporarily prolonging the time until ejaculation

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

INGREDIENTS AND APPEARANCE

DZEUS CLIMAX CONTROL WIPES 
benzocaine cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54723-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	7 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54723-006-01	3 mL in 1 POUCH; Type 0: Not a Combination Product	12/08/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/08/2021

Labeler - Sambria Pharmaceuticals, LLC (078676259)