NDC Package 63742-012-00 Numb520

Lidocaine Hydrochloride,Phenylephrine Hydrochloride Spray 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:
63742-012-00
Package Description:
72 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Numb520
Non-Proprietary Name:
Lidocaine Hydrochloride, Phenylephrine Hydrochloride
Substance Name:
Lidocaine Hydrochloride; Phenylephrine Hydrochloride
Usage Information:
Clean the affected area.sensitivity and possible allergy tests advised prior to use. Spray spraingly to affected area after thoroughly cleansing. Wait until anesthetic effect occurs. You may reapply to continue numbing effect.apply to the affected area up to 4 times daily.children under 12 years of age, consult a doctor.
11-Digit NDC Billing Format:
63742001200
NDC to RxNorm Crosswalk:
  • RxCUI: 2168528 - lidocaine HCl 5 % / phenylephrine HCl 0.25 % Topical Spray
  • RxCUI: 2168528 - lidocaine hydrochloride 50 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Topical Spray
  • RxCUI: 2168528 - lidocaine hydrochloride 5 % / phenylephrine hydrochloride 0.25 % Topical Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Clinical Resolution Laboratory, Inc.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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:
    05-01-2019
    Listing Expiration Date:
    12-31-2024
    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 63742-012-00?

    The NDC Packaged Code 63742-012-00 is assigned to a package of 72 ml in 1 bottle of Numb520, a human over the counter drug labeled by Clinical Resolution Laboratory, Inc.. The product's dosage form is spray and is administered via topical form.

    Is NDC 63742-012 included in the NDC Directory?

    Yes, Numb520 with product code 63742-012 is active and included in the NDC Directory. The product was first marketed by Clinical Resolution Laboratory, Inc. on May 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 63742-012-00?

    The 11-digit format is 63742001200. 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
    5-3-263742-012-005-4-263742-0012-00