Purell Hand Sanitizing Wipes Alcohol Formula Cloth
NDC Package 21749-367-94
Package Information
Purell Hand Sanitizing Wipes Alcohol Formula (alcohol) cloths is • Wet hands thoroughly with product and allow to dry • Children under 6 years of age should be supervised when using PURELL® products. This formulation utilizes a cloth delivery system. Marketed by Gojo Industries, Inc., this product is identified by NDC 21749-367 and is authorized under FDA application 505G(a)(3).
Identification & Billing
- RxCUI: 1041780 - ethanol 62 % Medicated Pad
- RxCUI: 1041780 - ethanol 0.62 ML/ML Medicated Pad
- RxCUI: 1041780 - ethanol 62 % Hand Sanitizer Wipes
- RxCUI: 1041780 - ethanol 62 % Topical Cloth
- RxCUI: 1041780 - ethanol 62 % Topical Swab
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 21749 - Gojo Industries, Inc.
- 21749-367 - Purell Hand Sanitizing Wipes Alcohol Formula
- 21749-367-94 - 135 PACKAGE in 1 PACKAGE / 370 mL in 1 PACKAGE
- 21749-367 - Purell Hand Sanitizing Wipes Alcohol Formula
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 (21749-367). Click a package code to view its specific billing and regulatory data.
* 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 21749-367-94 identifies a specific commercial package of 135 package in 1 package / 370 ml in 1 package of Purell Hand Sanitizing Wipes Alcohol Formula, a human over the counter drug labeled by Gojo Industries, Inc.. This cloth is formulated for topical use and contains alcohol as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Gojo Industries, Inc. on February 24, 2012. The current certification is valid through December 31, 2026.
How is this Gojo Industries, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 21749036794. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.