Skip to Content
Print Save

Climax Control Benzocaine

Medically reviewed by Drugs.com. Last updated on Oct 12, 2020.

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

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

Further information

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

Medical Disclaimer