NDC Package 80948-014-27 Puroma Antibacterial Foaming Hand Wash With Fragrance Alcohol Free Citrus Floral

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:
80948-014-27
Package Description:
4 BOTTLE in 1 PACKAGE / 250 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Puroma Antibacterial Foaming Hand Wash With Fragrance Alcohol Free Citrus Floral
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:
80948001427
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:
    04-23-2021
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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
    80948-014-014 BOTTLE in 1 PACKAGE / 70 mL in 1 BOTTLE
    80948-014-026 BOTTLE in 1 PACKAGE / 70 mL in 1 BOTTLE
    80948-014-038 BOTTLE in 1 PACKAGE / 70 mL in 1 BOTTLE
    80948-014-0412 BOTTLE in 1 PACKAGE / 70 mL in 1 BOTTLE
    80948-014-0524 BOTTLE in 1 PACKAGE / 70 mL in 1 BOTTLE
    80948-014-064 BOTTLE in 1 PACKAGE / 100 mL in 1 BOTTLE
    80948-014-076 BOTTLE in 1 PACKAGE / 100 mL in 1 BOTTLE
    80948-014-088 BOTTLE in 1 PACKAGE / 100 mL in 1 BOTTLE
    80948-014-0912 BOTTLE in 1 PACKAGE / 100 mL in 1 BOTTLE
    80948-014-1024 BOTTLE in 1 PACKAGE / 100 mL in 1 BOTTLE
    80948-014-114 BOTTLE in 1 PACKAGE / 150 mL in 1 BOTTLE
    80948-014-126 BOTTLE in 1 PACKAGE / 150 mL in 1 BOTTLE
    80948-014-138 BOTTLE in 1 PACKAGE / 150 mL in 1 BOTTLE
    80948-014-1412 BOTTLE in 1 PACKAGE / 150 mL in 1 BOTTLE
    80948-014-1524 BOTTLE in 1 PACKAGE / 150 mL in 1 BOTTLE
    80948-014-164 BOTTLE in 1 PACKAGE / 200 mL in 1 BOTTLE
    80948-014-176 BOTTLE in 1 PACKAGE / 200 mL in 1 BOTTLE
    80948-014-188 PACKAGE in 1 PACKAGE / 200 mL in 1 PACKAGE
    80948-014-1912 BOTTLE in 1 PACKAGE / 200 mL in 1 BOTTLE
    80948-014-2024 BOTTLE in 1 PACKAGE / 200 mL in 1 BOTTLE
    80948-014-214 BOTTLE in 1 PACKAGE / 220 mL in 1 BOTTLE
    80948-014-226 BOTTLE in 1 PACKAGE / 220 mL in 1 BOTTLE
    80948-014-238 BOTTLE in 1 PACKAGE / 220 mL in 1 BOTTLE
    80948-014-2412 BOTTLE in 1 PACKAGE / 220 mL in 1 BOTTLE
    80948-014-2524 BOTTLE in 1 PACKAGE / 220 mL in 1 BOTTLE
    80948-014-262 BOTTLE in 1 PACKAGE / 250 mL in 1 BOTTLE
    80948-014-286 BOTTLE in 1 PACKAGE / 250 mL in 1 BOTTLE
    80948-014-298 PACKAGE in 1 PACKAGE / 250 mL in 1 PACKAGE
    80948-014-3012 BOTTLE in 1 PACKAGE / 250 mL in 1 BOTTLE
    80948-014-3124 BOTTLE in 1 PACKAGE / 250 mL in 1 BOTTLE
    80948-014-322 BOTTLE in 1 PACKAGE / 300 mL in 1 BOTTLE
    80948-014-334 BOTTLE in 1 PACKAGE / 300 mL in 1 BOTTLE
    80948-014-346 BOTTLE in 1 PACKAGE / 300 mL in 1 BOTTLE
    80948-014-358 BOTTLE in 1 PACKAGE / 300 mL in 1 BOTTLE
    80948-014-3612 PACKAGE in 1 PACKAGE / 300 mL in 1 PACKAGE
    80948-014-3724 BOTTLE in 1 PACKAGE / 300 mL in 1 BOTTLE
    80948-014-445000 mL in 1 CAN
    80948-014-4550000 mL in 1 CAN
    80948-014-46200000 mL in 1 DRUM
    80948-014-47250 mL in 1 BOTTLE
    80948-014-482 BOTTLE in 1 PACKAGE / 350 mL in 1 BOTTLE
    80948-014-494 BOTTLE in 1 PACKAGE / 350 mL in 1 BOTTLE
    80948-014-506 BOTTLE in 1 PACKAGE / 350 mL in 1 BOTTLE
    80948-014-518 BOTTLE in 1 PACKAGE / 350 mL in 1 BOTTLE
    80948-014-5212 BOTTLE in 1 PACKAGE / 350 mL in 1 BOTTLE
    80948-014-53250 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 80948-014-27?

    The NDC Packaged Code 80948-014-27 is assigned to a package of 4 bottle in 1 package / 250 ml in 1 bottle of Puroma Antibacterial Foaming Hand Wash With Fragrance Alcohol Free Citrus Floral, 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 80948-014 included in the NDC Directory?

    Yes, Puroma Antibacterial Foaming Hand Wash With Fragrance Alcohol Free Citrus Floral with product code 80948-014 is active and included in the NDC Directory. The product was first marketed by Zenith Micro Control on April 23, 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 80948-014-27?

    The 11-digit format is 80948001427. 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
    5-3-280948-014-275-4-280948-0014-27