DYNAMO DELAY- lidocaine spray

DYNAMO DELAY by

Drug Labeling and Warnings

DYNAMO DELAY by is a Otc medication manufactured, distributed, or labeled by Momentum Management LLC, Westwood Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

INGREDIENTS AND APPEARANCE

DYNAMO DELAY 
lidocaine spray

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

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69664-001-01	1 in 1 BOX	05/13/2015
1		22.2 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

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	Business Operations
Westwood Laboratories Inc		832280635	manufacture(69664-001)