FDA.reportPublic FDA data

Dynamo Wellness Delay Wipe

Manufacturer
Momentum Management LLC | Diamond Wipes International, Inc
Effective date
2026-01-08
Label type
Human OTC Drug Label
Version
3
Source
full-release
Hydrated at
2026-06-01 01:35:05

Label at a glance#

ProductDynamo Wellness Delay Wipe
Active ingredientBENZOCAINE
Label structure9 sections

Dosage and administration

Open the packet, remove the wipe, and gently wipe the head of the shaft of penis before intercourse. Allow at least 5 minutes to dry. Wash product off after intercourse.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 4%

PURPOSE

OTC - PURPOSE SECTION

External Analgesic 

USE(S)

INDICATIONS & USAGE SECTION

Helps in temporarily prolonging the time until ejaculation.

WARNINGS

WARNINGS SECTION

● For external use only.
● When using this product, avoid contact with eyes.

STOP USE AND ASK DOCTOR IF

OTC - STOP USE SECTION

● This product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical 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.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Alcohol, Denatonium Benzoate, Propylene Glycol, t-Butyl Alcohol, Water.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Open the packet, remove the wipe, and gently wipe the head of the shaft of penis before intercourse. Allow at least 5 minutes to dry. Wash product off after intercourse.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

delay-wipedelay-wipe

Packaging Details
● Package Type: Individually Wrapped Wipe
● Quantity: 1 wipe per package
● Size: 2.375 inch x 3 inch foil

Manufactured For

Momentum Management LLC

1206 West Jon Street

Torrance, CA. 90502

+1 310 446-1632

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1491009benzocaine 4 % Medicated PadPSN3
1491009benzocaine 40 MG/ML Medicated PadSCD3
1491009benzocaine 4 % Medicated PadSY3

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
69664-005-01Dynamo Wellness Delay Wipe1 g in 1 PACKETCLOTH13
69664-005-02Dynamo Wellness Delay Wipe6 in 1 PACKAGECLOTH63
69664-005-02Dynamo Wellness Delay Wipe1 g in 1 PACKETCLOTH13
69664-005-03Dynamo Wellness Delay Wipe18 in 1 PACKAGECLOTH183
69664-005-03Dynamo Wellness Delay Wipe1 g in 1 PACKETCLOTH13
69664-005-04Dynamo Wellness Delay Wipe1 g in 1 PACKETCLOTH13
69664-005-04Dynamo Wellness Delay Wipe36 in 1 PACKAGECLOTH363

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69664-00569664-005-01, 69664-005-02, 69664-005-03, 69664-005-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOCAINEU3RSY48JW5ACTIB
ALCOHOL3K9958V90MIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BUTYL ALCOHOL8PJ61P6TS3IACT
WATER059QF0KO0RIACT

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
Dynamo Wellness Delay WipeDYNAMO WELLNESS DELAY WIPEMomentum Management LLCb4319333-3c8d-40ab-ab70-99de1abbe8712026-01-08WarningsExact identifier
ndc (package): 69664-005-04
ndc (package): 69664-005-01
ndc (package): 69664-005-03
ndc (package): 69664-005-02
ndc (product): 69664-005
ndc11 (package): 69664000501
ndc11 (package): 69664000502
ndc11 (package): 69664000503
ndc11 (package): 69664000504
spl id: 1b37aef3-c93f-427e-a11f-cf7d54684303
spl set id: b4319333-3c8d-40ab-ab70-99de1abbe871

Reported adverse events (FAERS/openFDA)#

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