FDA.reportPublic FDA data

Desensitizing cream

Manufacturer
I Shay Cosmetics Inc
Effective date
2022-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:52:05

Label at a glance#

ProductDesensitizing cream
Active ingredientBENZOCAINE
Label structure8 sections

Dosage and administration

Apply a small amount 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#

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 5% .... Male Genital Desensitizer

OTC - PURPOSE SECTION

Male Genital Desensitizer

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

WARNINGS - Keep out of reach of children

INDICATIONS & USAGE SECTION

For temporary male genital desensitization, helping to slow the onset of ejaculation.

INACTIVE INGREDIENT SECTION

Deionized Water, Propylene Glycol, Coconut Oil, Stearic Acid, Isopropyl Palmitate, Capric/Caprylic Triglyceride, Soya Oil, Cetyl Alcohol, Cetearyl Alcohol, Ceteareth-20 Glycol Stearate, Dimethicone 100, PEG-100, Sodium Hydroxide, Carbomer, Phenoxyethanol, Propylparaben, Methylparaben, Fragrance.

WARNINGS SECTION

Premature ejaculation may be due to a condition requiring medical supervision. If this product, used as directed, does not provide relief, discontinue use and consult a physician.

Keep out of reach of children.

If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor. Avoid contact with the eyes.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply a small amount to head and shaft of penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label banzocainelabel banzocaine

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65112-20965112-209-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZOCAINEU3RSY48JW5ACTIB

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
ea7aa07c-5a3e-d16b-e053-2a95a90a9d9fb9e48f11-a6f8-4de4-e053-2a95a90a81ee2022-10-07WarningsExact identifier
spl id: ea7aa07c-5a3e-d16b-e053-2a95a90a9d9f
spl set id: b9e48f11-a6f8-4de4-e053-2a95a90a81ee

Reported adverse events (FAERS/openFDA)#

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