NDC Package 80948-006-06 Puroma Antibacterial Hand Wash Fragrance Free

Benzalkonium Chloride 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:
80948-006-06
Package Description:
2 BOTTLE in 1 PACKAGE / 237 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Puroma Antibacterial Hand Wash Fragrance Free
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
• Wet hands and wrists with clean running water • Apply appropriate amount of product • Lather and scrub hands, fingers, fingernails, cuticles and wrists thoroughly • Rinse thoroughly with running water • Dry hands completely.
11-Digit NDC Billing Format:
80948000606
NDC to RxNorm Crosswalk:
  • RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Zenith Micro Control
    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:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-05-2021
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    80948-006-074 BOTTLE in 1 PACKAGE / 237 mL in 1 BOTTLE
    80948-006-086 BOTTLE in 1 PACKAGE / 237 mL in 1 BOTTLE
    80948-006-098 BOTTLE in 1 PACKAGE / 237 mL in 1 BOTTLE
    80948-006-1012 BOTTLE in 1 PACKAGE / 237 mL in 1 BOTTLE
    80948-006-1124 BOTTLE in 1 PACKAGE / 237 mL in 1 BOTTLE
    80948-006-122 BOTTLE in 1 PACKAGE / 326 mL in 1 BOTTLE
    80948-006-134 BOTTLE in 1 PACKAGE / 326 mL in 1 BOTTLE
    80948-006-146 BOTTLE in 1 PACKAGE / 326 mL in 1 BOTTLE
    80948-006-158 BOTTLE in 1 PACKAGE / 326 mL in 1 BOTTLE
    80948-006-1612 BOTTLE in 1 PACKAGE / 326 mL in 1 BOTTLE
    80948-006-1724 BOTTLE in 1 PACKAGE / 326 mL in 1 BOTTLE
    80948-006-182 BOTTLE in 1 PACKAGE / 474 mL in 1 BOTTLE
    80948-006-194 BOTTLE in 1 PACKAGE / 474 mL in 1 BOTTLE
    80948-006-206 BOTTLE in 1 PACKAGE / 474 mL in 1 BOTTLE
    80948-006-218 BOTTLE in 1 PACKAGE / 474 mL in 1 BOTTLE
    80948-006-2212 BOTTLE in 1 PACKAGE / 474 mL in 1 BOTTLE
    80948-006-2324 BOTTLE in 1 PACKAGE / 474 mL in 1 BOTTLE
    80948-006-242 BOTTLE in 1 PACKAGE / 947 mL in 1 BOTTLE
    80948-006-254 BOTTLE in 1 PACKAGE / 947 mL in 1 BOTTLE
    80948-006-265000 mL in 1 CAN
    80948-006-2750000 mL in 1 CAN
    80948-006-28200000 mL in 1 DRUM
    80948-006-294 BOTTLE in 1 PACKAGE / 178 mL in 1 BOTTLE
    80948-006-306 BOTTLE in 1 PACKAGE / 178 mL in 1 BOTTLE
    80948-006-318 BOTTLE in 1 PACKAGE / 178 mL in 1 BOTTLE
    80948-006-3212 BOTTLE in 1 PACKAGE / 178 mL in 1 BOTTLE
    80948-006-3324 BOTTLE in 1 PACKAGE / 178 mL in 1 BOTTLE
    80948-006-34178 mL in 1 BOTTLE
    80948-006-35237 mL in 1 BOTTLE
    80948-006-36326 mL in 1 BOTTLE
    80948-006-37474 mL in 1 BOTTLE
    80948-006-38974 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 80948-006-06?

    The NDC Packaged Code 80948-006-06 is assigned to a package of 2 bottle in 1 package / 237 ml in 1 bottle of Puroma Antibacterial Hand Wash Fragrance Free, a human over the counter drug labeled by Zenith Micro Control. The product's dosage form is liquid and is administered via topical form.

    Is NDC 80948-006 included in the NDC Directory?

    Yes, Puroma Antibacterial Hand Wash Fragrance Free with product code 80948-006 is active and included in the NDC Directory. The product was first marketed by Zenith Micro Control on March 05, 2021 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 80948-006-06?

    The 11-digit format is 80948000606. 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
    5-3-280948-006-065-4-280948-0006-06