Jumbo Wipes
NDC Package 81071-001-04

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Jumbo Wipes is pull cloth our of opening & wipe hands thoroughly. Discard used wipe in trash receptacle, do not flush. Children under 6 years of age should be supervised when using this product. Close package after each us. Marketed by Quikit Limited, this product is identified by NDC 81071-001 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
81071-001-04
Package Description
1000 NOT APPLICABLE in 1 PACKAGE / 2.07 mL in 1 NOT APPLICABLE
Product Code
81071-001
11-Digit Billing Format
81071000104
RxNorm Crosswalk
  • RxCUI: 2464106 - ethanol 71.25 % / isopropyl alcohol 3.75 % Medicated Pad
  • RxCUI: 2464106 - ethanol 0.713 ML/ML / isopropyl alcohol 0.0375 ML/ML Medicated Pad

Clinical Specifications

Proprietary Name
Jumbo Wipes
Dosage Form
-
Usage Information
Pull cloth our of opening & wipe hands thoroughly. Discard used wipe in trash receptacle, do not flush. Children under 6 years of age should be supervised when using this product. Close package after each us.

Regulatory & Marketing

Labeler Name
Quikit Limited
FDA Application #
part333A
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
11-15-2020
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 (81071-001). Click a package code to view its specific billing and regulatory data.

81071-001-01
250 NOT APPLICABLE in 1 PACKAGE / 2.07 mL in 1 NOT APPLICABLE
81071-001-02
500 NOT APPLICABLE in 1 PACKAGE / 2.07 mL in 1 NOT APPLICABLE
81071-001-03
800 NOT APPLICABLE in 1 PACKAGE / 2.07 mL in 1 NOT APPLICABLE
81071-001-05
1200 NOT APPLICABLE in 1 PACKAGE / 2.07 mL in 1 NOT APPLICABLE

* 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 81071-001-04 identifies a specific commercial package of 1000 not applicable in 1 package / 2.07 ml in 1 not applicable of Jumbo Wipes, labeled by Quikit Limited. 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 Quikit Limited on November 15, 2020. The current certification is valid through December 31, 2021.

How is this Quikit Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81071000104. 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)
81071-001-04
11-Digit CMS (5-4-2)
81071-0001-04

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