Nuvik Large Roll Antibacterial Hand Wipes
NDC Package 74602-800-80

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

Package Information

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

Nuvik Large Roll Antibacterial Hand Wipes is adults and children2 years and overâ–ª apply to handsâ–ª allow to dry without wipingchildren under 2 yearsâ–ª ask a doctor before useTo Dispense: Look for tear-notch located at the top of the refill pouch. Marketed by Nuvik Usa, Inc., this product is identified by NDC 74602-800 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
74602-800-80
Package Description
800 PACKAGE in 1 BAG / 3.125 g in 1 PACKAGE
Product Code
74602-800
11-Digit Billing Format
74602080080
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Nuvik Large Roll Antibacterial Hand Wipes
Dosage Form
-
Usage Information
Adults and children2 years and overâ–ª apply to handsâ–ª allow to dry without wipingchildren under 2 yearsâ–ª ask a doctor before useTo Dispense: Look for tear-notch located at the top of the refill pouch. Open pouch by tearing straight across at notch. Starting from the center of the roll, pull one wipe through the pouch center opening and then thread wipe through the dispenser nozzle. Adjust nozzle tension on dispenser, if applicable. For use with upward-pull dispensers (floor stand or wall units) only; product will drip in a downward-pull dispenser.For Use: Pull wipe up from the dispenser feed at an angle and tear from roll with a downward motion. Wipe surface thoroughly and allow to dry naturally. Dispose of wipe in trash.

Regulatory & Marketing

Labeler Name
Nuvik Usa, Inc.
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
05-01-2020
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 74602-800-80 identifies a specific commercial package of 800 package in 1 bag / 3.125 g in 1 package of Nuvik Large Roll Antibacterial Hand Wipes, labeled by Nuvik Usa, 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 Nuvik Usa, Inc. on May 01, 2020. The current certification is valid through December 31, 2021.

How is this Nuvik Usa, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 74602080080. 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)
74602-800-80
11-Digit CMS (5-4-2)
74602-0800-80

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