DYNAMO DELAY SAMPLE BOTTLE- lidocaine spray

DYNAMO DELAY SAMPLE BOTTLE by

Drug Labeling and Warnings

DYNAMO DELAY SAMPLE BOTTLE 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

USE(S)

• 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

Dynamo Delay
NDC: 69664-003-02
Lidocaine USP 13%
(approximately 10 mg per spray)
Male Genital Desensitizer Spray
Helps in temporarily prolonging the time until ejaculation.
.088 fl oz (2.6mL)
Made in the USA

INGREDIENTS AND APPEARANCE

DYNAMO DELAY SAMPLE BOTTLE 
lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69664-003
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: 69664-003-02	1 in 1 BOX	05/31/2024
1		2.6 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		05/31/2024

Labeler - Momentum Management LLC (828734397)

Registrant - Westwood Laboratories, LLC (832280635)

Establishment
Name	Address	ID/FEI	Business Operations
Westwood Laboratories, LLC		832280635	LABEL(69664-003) , MANUFACTURE(69664-003) , PACK(69664-003)