NDC Package 49687-0017-0 Refill 3

Benzalkonium Chloride,Lidocaine Hydrochloride Cream 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:
49687-0017-0
Package Description:
10 PACKAGE in 1 BOX / .9 g in 1 PACKAGE
Product Code:
Proprietary Name:
Refill 3
Non-Proprietary Name:
Benzalkonium Chloride, Lidocaine Hydrochloride
Substance Name:
Benzalkonium Chloride; Lidocaine Hydrochloride
Usage Information:
Clean the affected areaAdults and children 2 years of age and older: Apply a small amount of this product to affected area not more than 3 times dailyChildren under 2 years of age: consult a doctorMay be covered with a sterile bandage
11-Digit NDC Billing Format:
49687001700
NDC to RxNorm Crosswalk:
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cmc Group Inc.
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-10-2016
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49687-0017-0?

    The NDC Packaged Code 49687-0017-0 is assigned to a package of 10 package in 1 box / .9 g in 1 package of Refill 3, a human over the counter drug labeled by Cmc Group Inc.. The product's dosage form is cream and is administered via topical form.

    Is NDC 49687-0017 included in the NDC Directory?

    Yes, Refill 3 with product code 49687-0017 is active and included in the NDC Directory. The product was first marketed by Cmc Group Inc. on August 10, 2016 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 49687-0017-0?

    The 11-digit format is 49687001700. 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 5-4-1 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
    5-4-149687-0017-05-4-249687-0017-00