CLIMAX CONTROL BENZOCAINE- benzocaine gel

Climax Control by

Drug Labeling and Warnings

Climax Control by is a Otc medication manufactured, distributed, or labeled by Natureplex LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzocaine 7.5%

Purpose

Male genital desensitizer

Uses

• helps in temporarily prolonging time until ejaculation

Warnings

For external use only.

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 conditions requiring medical supervision
• you or your partner develop a rash or irritation, such as burning or itching

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Directions

• apply a small amount to head and shaft of penis before intercourse, or use as directed by a physician
• wash product off after intercourse

Other information

• store at 15 to 30°C (59 to 86°F)
• do not use if seal on tube is punctured or missing
• contents filled by weight, not volume

Inactive ingredients

hydroxypropylcellulose, PEG-8, propylene glycol

Questions or comments?

866-323-0107 or www.natureplex.com

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

Helps
Prolong
Sexual
Pleasure

MAXIMUM STRENGTH
DESENSITIZER
CLIMAX CONTROL GEL

NET WT. 1 Oz. (28g)

INGREDIENTS AND APPEARANCE

CLIMAX CONTROL   BENZOCAINE
benzocaine gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67234-038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5)	Benzocaine	0.075 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67234-038-01	1 in 1 CARTON	01/25/2016
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333B	01/25/2016

Labeler - Natureplex LLC (062808196)

Establishment
Name	Address	ID/FEI	Business Operations
Natureplex LLC		062808196	MANUFACTURE(67234-038)