NDC Package 72654-037-02 Numb520spray

Lidocaine,Phenylephrine Hcl Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
72654-037-02
Package Description:
72 mL in 1 BOTTLE, PUMP
Product Code:
Proprietary Name:
Numb520spray
Non-Proprietary Name:
Lidocaine, Phenylephrine Hcl
Substance Name:
Lidocaine; Phenylephrine Hydrochloride
Usage Information:
Uses■ For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders and anorectal inflammation.■ For the temporary relief of pain, burning and soreness.■ Temporarily shrinks hemorrhoidal tissue.■ Temporarily reduces the swelling associated with irritation in hemorrhoids and other anorectal disorders.
11-Digit NDC Billing Format:
72654003702
NDC to RxNorm Crosswalk:
  • RxCUI: 2590656 - lidocaine 5 % / phenylephrine hydrochloride 0.25 % Rectal Spray
  • RxCUI: 2590656 - lidocaine 50 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Rectal Spray
Product Type:
Human Otc Drug
Labeler Name:
Ebanel Laboratories, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Sample Package:
No
FDA Application Number:
M015
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-13-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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Frequently Asked Questions

What is NDC 72654-037-02?

The NDC Packaged Code 72654-037-02 is assigned to a package of 72 ml in 1 bottle, pump of Numb520spray, a human over the counter drug labeled by Ebanel Laboratories, Inc.. The product's dosage form is liquid and is administered via topical form.

Is NDC 72654-037 included in the NDC Directory?

Yes, Numb520spray with product code 72654-037 is active and included in the NDC Directory. The product was first marketed by Ebanel Laboratories, Inc. on May 13, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72654-037-02?

The 11-digit format is 72654003702. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-272654-037-025-4-272654-0037-02