FDA.reportPublic FDA data

Joydrops Climax Control Male Genital Desensitizer Spray

Manufacturer
Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS. | Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunleri Sanayi Ve Ticaret AS
Effective date
2025-08-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:34:54

Label at a glance#

ProductJoydrops Climax Control Male Genital Desensitizer
Active ingredientLIDOCAINE
Label structure7 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 10mg/spray

Purpose

OTC - PURPOSE SECTION

Male Genital Desensitizer

Use

INDICATIONS & USAGE SECTION

  • Helps in the prevention of premature ejaculation.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

SPL UNCLASSIFIED SECTION

  • Store at 20-25ºC (68-77ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73107-00573107-005-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
BENZYL ALCOHOLLKG8494WBHIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
WATER059QF0KO0RIACT
LIDOCAINE98PI200987ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3ce172eb-4e2f-8640-e063-6294a90a5328c8b4d0c1-0aab-4f11-a8bd-469d702873b12025-08-21WarningsExact identifier
spl id: 3ce172eb-4e2f-8640-e063-6294a90a5328
spl set id: c8b4d0c1-0aab-4f11-a8bd-469d702873b1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.