CLIMAX CONTROL  BENZOCAINE- benzocaine gel 
Natureplex LLC

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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Climax Control Gel
Benzocaine 7.5%

Drug Facts

Active ingredient

Benzocaine 7.5%

Purpose

Male genital desensitizer

Use

Helps in temporarily prolonging time until ejaculation

Warnings

Not for prolonged use.

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. If symptoms persist, consult a doctor.

If partner is pregnant or breast-feeding, ask a health professional before use.

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

Directions

Other information

Inactive ingredients

hydroxypropylcellulose, PEG 400, 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)

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
CLIMAX CONTROL   BENZOCAINE
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67234-038
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine0.075 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67234-038-011 in 1 CARTON01/25/2016
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333B01/25/2016
Labeler - Natureplex LLC (062808196)
Establishment
NameAddressID/FEIBusiness Operations
Natureplex LLC062808196MANUFACTURE(67234-038)

Revised: 7/2021
Document Id: 191f61b4-be43-4421-bc47-a0990edcba51
Set id: d1f959c7-fc6d-4e4d-ab15-9deceab1359a
Version: 3
Effective Time: 20210701
 
Natureplex LLC