Purell Professional Advanced Hand Sanitizer Fragrance Free Foam
NDC Package 21749-821-53

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Purell Professional Advanced Hand Sanitizer Fragrance Free Foam is a . Marketed by Gojo Industries, Inc., this product is identified by NDC 21749-821 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
21749-821-53
Package Description
535 mL in 1 PACKAGE
Product Code
11-Digit Billing Format
21749082153

Clinical Specifications

Proprietary Name
Purell Professional Advanced Hand Sanitizer Fragrance Free Foam
Dosage Form
-

Regulatory & Marketing

Labeler Name
Gojo Industries, Inc.
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-05-2017
End Marketing Date
05-31-2023
Listing Expiration
05-31-2023
Exclude Flag
D
Sample Package
No

Hierarchy 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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (21749-821). Click a package code to view its specific billing and regulatory data.

1200 mL in 1 PACKAGE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 21749-821-53 identifies a specific commercial package of 535 ml in 1 package of Purell Professional Advanced Hand Sanitizer Fragrance Free Foam, labeled by Gojo Industries, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Gojo Industries, Inc. on September 05, 2017. The current certification is valid through May 31, 2023.

How is this Gojo Industries, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 21749082153. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
21749-821-53
11-Digit CMS (5-4-2)
21749-0821-53

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.