FDA.reportPublic FDA data

5 Elementum Delay Wipes

Manufacturer
MSVenturesGroup OÜ | Zhejiang Shini Nursing Products Technology Co., Ltd
Effective date
2026-02-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:36:43

Label at a glance#

Product5 Elementum Delay Wipes
Active ingredientBENZOCAINE
Label structure1 sections

Label contents#

Full prescribing information#

Outer Package Label Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the retail outer box for 5 Elementum Delay Wipes (benzocaine wipes)Image of the retail outer box for 5 Elementum Delay Wipes (benzocaine wipes)

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Drug Facts


Active ingredient (in each wipe)
Benzocaine 7%

Purpose

OTC - PURPOSE SECTION

Male genital desensitizer

Uses

INDICATIONS & USAGE SECTION

Helps in reducing oversensitivity of the penile head during intercourse

Warnings ​Keep out of reach of children.

WARNINGS SECTION

For external use only. When using this product, avoid contact with eyes.
• This product is intended to be used as directed. Read and follow all directions and warnings provided.
• Stop use and ask a doctor if you or your partner develops rash or irritation.
• If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply a small amount to the head and shaft of the penis before intercourse. Allow 5 minutes for the product to dry.
• Wash hands completely after application.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Alcohol, Glycereth-26, Glycerin, Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Tocopheryl Acetate, Benzalkonium Chloride, Hyaluronic Acid, Citric Acid.

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

DailyMed Pharmacologic Classes#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87203-001-015 Elementum Delay Wipes10 in 1 BOXCLOTH103
87203-001-015 Elementum Delay Wipes1 g in 1 PACKAGECLOTH13
87203-001-025 Elementum Delay Wipes4 in 1 BOXCLOTH43
87203-001-025 Elementum Delay Wipes1 g in 1 PACKAGECLOTH13
87203-001-035 Elementum Delay Wipes1 g in 1 PACKAGECLOTH13
87203-001-035 Elementum Delay Wipes30 in 1 BOXCLOTH303

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87203-00187203-001-01, 87203-001-02, 87203-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONIC ACIDS270N0TRQYIACT
ALCOHOL3K9958V90MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
DIPROPYLENE GLYCOLE107L85C40IACT
CITRIC ACID2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
BENZOCAINEU3RSY48JW5ACTIB
AQUA059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
MATRICARIA CHAMOMILLA FLOWERING TOP3VNC7T6Z02IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-11-20monthly-update2026-06-03 17:45:04

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
5 Elementum Delay WipesBENZOCAINE DELAY WIPESMSVenturesGroup O440539b0-612b-3b41-e063-6294a90a1ddd2026-02-05WarningsExact identifier
ndc (package): 87203-001-03
ndc (package): 87203-001-02
ndc (package): 87203-001-01
ndc (product): 87203-001
ndc11 (package): 87203000103
ndc11 (package): 87203000102
ndc11 (package): 87203000101
spl id: 4a14e481-bab8-8eaf-e063-6394a90afb22
spl set id: 440539b0-612b-3b41-e063-6294a90a1ddd

Reported adverse events (FAERS/openFDA)#

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