DYNAMO DELAY: Package Insert and Label Information

DYNAMO DELAY- lidocaine spray
Momentum Management LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Lidocaine USP 13%

(approximately 10 mg per spray)


Topical Anesthetic


  • 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


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


  • 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


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

Outer Box
(click image for full-size original)

Bottle Label:

Bottle Label
(click image for full-size original)
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
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Multilevel Packaging
1 NDC:69664-001-01 1 BOTTLE, SPRAY in 1 BOX contains a BOTTLE, SPRAY
1 22.2 mL in 1 BOTTLE, SPRAY This package is contained within the BOX (69664-001-01)
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)
Name Address ID/FEI Operations
Westwood Laboratories Inc 832280635 manufacture (69664-001)

Revised: 01/2020 Momentum Management LLC

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