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 onl

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

Last Longer!

Prolong Your Pleasure!

DYNAMO DELAY

NDC 69664-002-01

Lidocaine USP 13%

(approximately 10mg per spray)

150+ sprays per bottle

Convenient pocket size

Helps in temporarily prolonging the time until ejaculation

Black Label Edition

1/2 fl oz (15mL)

Made in the USA

Bottle Label

Outer Box

DYNAMO DELAY BLACK LABEL
lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69664-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	10 mg in 0.08 mL

Ingredient Name	Strength
Inactive Ingredients
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
STEARIC ACID (UNII: 4ELV7Z65AP)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69664-002-01	1 in 1 BOX	01/01/2018	06/01/2022
1		15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	part335	01/01/2018	06/01/2022

Labeler - Momentum Management LLC (828734397)

Name	Address	ID/FEI	Business Operations
Establishment
Westwood Laboratories, LLC		832280635	LABEL(69664-002) , MANUFACTURE(69664-002) , PACK(69664-002)

Revised: 4/2024

Document Id: 33f1a7c2-22c9-4184-914e-f4dccf45b0df

Set id: 6bca20ca-52fe-30f9-e053-2a91aa0a9dd4

Version: 4

Effective Time: 20240417

Momentum Management LLC