NDC Package 37000-602-40 Safeguard Antibacterial E2 Foaming

Benzalkonium Chloride Soap 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:
37000-602-40
Package Description:
1200 mL in 1 BAG
Product Code:
Proprietary Name:
Safeguard Antibacterial E2 Foaming
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Wet hands and forearmsApply enough product to adequately cover the entire surfaces of the hands and forearmsScrub thoroughly for at least 30 seconds (include the fingernails and the cuticles)Rinse
11-Digit NDC Billing Format:
37000060240
NDC to RxNorm Crosswalk:
  • RxCUI: 1053188 - benzalkonium chloride 0.12 % Medicated Liquid Soap
  • RxCUI: 1053188 - benzalkonium chloride 1.2 MG/ML Medicated Liquid Soap
  • RxCUI: 1053192 - Safeguard Antibacterial Foaming 0.12 % Medicated Liquid Soap
  • RxCUI: 1053192 - benzalkonium chloride 1.2 MG/ML Medicated Liquid Soap [Safeguard Antibacterial Foaming]
  • RxCUI: 1053192 - Safeguard Antibacterial Foaming 1.2 MG/ML Medicated Liquid Soap
  • Product Type:
    Human Otc Drug
    Labeler Name:
    The Procter & Gamble Manufacturing Company
    Dosage Form:
    Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    M005
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    07-01-2010
    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 37000-602-40?

    The NDC Packaged Code 37000-602-40 is assigned to a package of 1200 ml in 1 bag of Safeguard Antibacterial E2 Foaming, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is soap and is administered via topical form.

    Is NDC 37000-602 included in the NDC Directory?

    Yes, Safeguard Antibacterial E2 Foaming with product code 37000-602 is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on July 01, 2010 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 37000-602-40?

    The 11-digit format is 37000060240. 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
    5-3-237000-602-405-4-237000-0602-40