DYNAMO DELAY

Dosage form: spray
Ingredients: LIDOCAINE 10mg in 0.08mL
Labeler: Momentum Management LLC
NDC code: 69664-001

Medically reviewed by Drugs.com. Last updated on Jan 1, 2024.

Active Ingredient

Lidocaine USP 13%

(approximately 10 mg per spray)

Purpose

Topical Anesthetic

Uses

for temporary male genital desensitization, helping to slow the onset of ejaculation
helps in temporarily prolonging the time until ejaculation
for reducing oversensitivity in the male in advance of intercourse

Warnings

For external use only

When using this product

avoid contact with the eyes

Stop use and ask a doctor if:

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.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

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

Inactive Ingredients

Isopropyl Palmitate, SD Alcohol 40B, Stearic Acid

Questions?

310 446 1632 Monday - Friday 9am-5pm(PST)

Manufactured for

Momentum Management LLC

1206 W Jon St

Torrance, CA 90502

Principal Display Panel

Screaming O

Dynamo Delay

NDC 69664-001-01

Lidocaine USP 13%

(appromixately 10 mg per spray)

Male Genital Desensitizer Spray

Helps in temporarily prolonging the time until ejaculation

3/4 fl oz (22.2mL)

Made in the USA

Bottle Label:

DYNAMO DELAY
lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69664-001
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (LIDOCAINE)	LIDOCAINE	10 mg in 0.08 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL PALMITATE
ALCOHOL
STEARIC ACID

Packaging
#	Item Code	Package Description
1	NDC:69664-001-01	1 BOTTLE, SPRAY in 1 BOX
1		22.2 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	05/13/2015

Labeler - Momentum Management LLC (828734397)

Establishment
Name	Address	ID/FEI	Operations
Westwood Laboratories Inc		832280635	manufacture(69664-001)

Revised: 01/2020

Document Id: 9bdf46d3-88f8-bb29-e053-2a95a90a82ef

Set id: 2ad63160-4f6f-4970-80b6-f6d19c5660a5

Version: 3

Effective Time: 20200111

Momentum Management LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer