Intimate Wipe

Manufacturer
Veru Inc. | Safetec of America, Inc.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:25

Label at a glance#

ProductIntimate Wipe
Active ingredientbenzocaine
Label structure9 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#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine USP 4%

Purpose

OTC - PURPOSE SECTION

Male Genital Desensitizer

Use

INDICATIONS & USAGE SECTION

Helps in temporarily prolonging time until ejaculation

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

ethyl alcohol (SDA 40B), propylene glycol, purified water

Principal Display Panel – Box Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PLAYBOY

INTIMATE WIPES

MALE GENITAL DESENSITIZER

Alright, Alright, All Night

Climax Delaying

Benzocaine Formulation

Fragrance & Paraben-Free

4 INDIVIDUALLY WRAPPED
CLIMAX DELAYING WIPES

Figure
Figure

Principal Display Panel – Packet Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PLAYBOY

INTIMATE WIPES

MALE GENITAL DESENSITIZER

1 INDIVIDUALLY WRAPPED

CLIMAX DELAYING WIPE

Figure
Figure

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130818546018577GTIN-13: 0818546018577
EAN-13: 0818546018577
GTIN-12: 818546018577
UPC-A: 818546018577
GTIN storage (14 digits): 00818546018577
pla02-0000-01.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69681-434-042022-01-28C16284748780-1d6a99b39-db50-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69681-434-04Intimate Wipe1.2 mL in 1 PACKETLIQUID1.21
69681-434-04Intimate Wipe4 in 1 BOXLIQUID41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69681-434INTIMATE WIPE (BENZOCAINE) LIQUID [VERU INC.]1Legacy NDC, 2 package rows20200608_48756768-4865-666e-6572-4c6976657321.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69681-43469681-434-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
23cd886e-a975-42ec-baf5-6cbacf805d6648756768-4865-666e-6572-4c69766573212020-06-08WarningsExact identifier
spl id: 23cd886e-a975-42ec-baf5-6cbacf805d66
spl set id: 48756768-4865-666e-6572-4c6976657321

Reported adverse events (FAERS/openFDA)#

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