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Climax Control Benzocaine

Dosage form: gel
Ingredients: Benzocaine 0.075g in 1g
Labeler: Natureplex LLC
NDC Code: 67234-038

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.

Climax Control Gel
Benzocaine 7.5%

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)

CLIMAX CONTROL   BENZOCAINE
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67234-038
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzocaine (Benzocaine) Benzocaine0.075 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
HYDROXYPROPYL CELLULOSE, UNSPECIFIED 
POLYETHYLENE GLYCOL 400 
PROPYLENE GLYCOL 
Packaging
#Item CodePackage Description
1NDC:67234-038-011 TUBE in 1 CARTON
128 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333B01/25/2016
Labeler - Natureplex LLC (062808196)
Establishment
NameAddressID/FEIOperations
Natureplex LLC062808196MANUFACTURE(67234-038)

Document Id: 8269c8c7-b6c3-45dc-a5e7-ffdefafcef2f
Set id: d1f959c7-fc6d-4e4d-ab15-9deceab1359a
Version: 2
Effective Time: 20171020
 
Natureplex LLC

Medically reviewed on Oct 20, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

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