Joydrops Climax Control Male Genital Desensitizer Spray

Joydrops Climax Control Male Genital Desensitizer by

Drug Labeling and Warnings

Joydrops Climax Control Male Genital Desensitizer by is a Otc medication manufactured, distributed, or labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS., Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

JOYDROPS CLIMAX CONTROL MALE GENITAL DESENSITIZER- lidocaine spray 
Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS.

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Joydrops Climax Control Male Genital Desensitizer Spray

Drug Facts

Active ingredient

Lidocaine 10mg/spray

Purpose

Male Genital Desensitizer

Use

  • Helps in the prevention of premature ejaculation.

Warnings

For external use only.

When using this product

  • Avoid contact with the eyes

Stop use and ask a doctor if

  • you or your partner develop a rash or irritation, such as burning or itching
  • this product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply 3 or more sprays, not to exceed 10, to head and shaft of penis before intercourse, or use as directed by a doctor.
  • Wash product off after intercourse.

Other information

  • Store at 20-25ºC (68-77ºF)

Inactive ingredients

Alcohol, Benzyl Alcohol, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Water

Package Labeling:

Outer PackageInner Package

JOYDROPS CLIMAX CONTROL MALE GENITAL DESENSITIZER 
lidocaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73107-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73107-005-011 in 1 BOX08/18/2025
110 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/18/2025
Labeler - Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS. (356325295)
Registrant - Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS. (356325295)
Establishment
NameAddressID/FEIBusiness Operations
Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS356325295manufacture(73107-005)

Revised: 8/2025
Document Id: 3ce172eb-4e2f-8640-e063-6294a90a5328
Set id: c8b4d0c1-0aab-4f11-a8bd-469d702873b1
Version: 2
Effective Time: 20250821
 
Turkuaz Saglik Hizmetleri Medikal Temizlik
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