NDC Package 21749-028-01 Purell Advanced Hand Sanitizer Be Vibrant

Alcohol Gel 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:
21749-028-01
Package Description:
30 mL in 1 PACKAGE
Product Code:
Proprietary Name:
Purell Advanced Hand Sanitizer Be Vibrant
Non-Proprietary Name:
Alcohol
Substance Name:
Alcohol
Usage Information:
Place enough product in your palm to thoroughly cover your handsRub hands together briskly until dryChildren under 6 years of age shodl be supervised when using this product
11-Digit NDC Billing Format:
21749002801
NDC to RxNorm Crosswalk:
  • RxCUI: 581662 - ethanol 70 % Topical Gel
  • RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
  • RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Gojo Industries, Inc.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    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:
    part333E
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    12-22-2016
    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
    21749-028-0259 mL in 1 PACKAGE
    21749-028-04118 mL in 1 PACKAGE
    21749-028-08236 mL in 1 PACKAGE
    21749-028-10295 mL in 1 PACKAGE
    21749-028-12354 mL in 1 PACKAGE
    21749-028-16473 mL in 1 PACKAGE
    21749-028-20591 mL in 1 PACKAGE
    21749-028-45450 mL in 1 PACKAGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 21749-028-01?

    The NDC Packaged Code 21749-028-01 is assigned to a package of 30 ml in 1 package of Purell Advanced Hand Sanitizer Be Vibrant, a human over the counter drug labeled by Gojo Industries, Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 21749-028 included in the NDC Directory?

    Yes, Purell Advanced Hand Sanitizer Be Vibrant with product code 21749-028 is active and included in the NDC Directory. The product was first marketed by Gojo Industries, Inc. on December 22, 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 21749-028-01?

    The 11-digit format is 21749002801. 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
    5-3-221749-028-015-4-221749-0028-01