What is NDC 69664-001?

69664-001 is the product NDC for Dynamo Delay (lidocaine), Lidocaine 10 mg/.08mL spray, listed with the FDA by Momentum Management LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Momentum Management LLC, NDC labeler code 69664. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dynamo Delay?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dynamo Delay NDC 69664-001 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69664-001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69664-0001Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
69664-001-02	69664000102	1 BOTTLE, SPRAY in 1 BOX (69664-001-02) / 22.2 mL in 1 BOTTLE, SPRAYMarketed from May 10, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dynamo Delay
Generic name (nonproprietary): lidocaine
Active ingredients: Lidocaine — 10 mg/.08mL
Dosage form: Spray
Route: Topical
Labeler: Momentum Management LLCNDC labeler code 69664
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: May 13, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 69664-001_570a530a-cbff-47c0-ab87-d67df54a822dSPL ID 570a530a-cbff-47c0-ab87-d67df54a822dSPL set ID 2ad63160-4f6f-4970-80b6-f6d19c5660a5UNII 98PI200987UPC 0817483011528
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N469664000102 followed by a unit qualifier and the quantity

Package 69664-0001-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 3, 2025.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69664-001

What is NDC 69664-001?: 69664-001 is the product NDC for Dynamo Delay (lidocaine), Lidocaine 10 mg/.08mL spray, listed with the FDA by Momentum Management LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dynamo Delay (Lidocaine).
What is the active ingredient?: Lidocaine.
Who is the labeler?: Momentum Management LLC, NDC labeler code 69664. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dynamo Delay?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Dynamo Delay (Lidocaine) NDC 69664-001