Alcohol Wipes
NDC Package 81648-001-01

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.

Alcohol Wipes is wet hands thoroughly with wipes, rub hands together until dry. Marketed by Zhejiang Dianfeng Industrial Co., Ltd., this product is identified by NDC 81648-001 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
81648-001-01
Package Description
10 PACKET in 1 BAG / 3.5 mL in 1 PACKET
Product Code
81648-001
11-Digit Billing Format
81648000101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Alcohol Wipes
Dosage Form
-
Usage Information
Wet hands thoroughly with wipes, rub hands together until dry

Regulatory & Marketing

Labeler Name
Zhejiang Dianfeng Industrial Co., Ltd.
FDA Application #
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
03-05-2021
Listing Expiration
12-31-2022
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 81648-001-01 identifies a specific commercial package of 10 packet in 1 bag / 3.5 ml in 1 packet of Alcohol Wipes, labeled by Zhejiang Dianfeng Industrial Co., Ltd.. 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 Zhejiang Dianfeng Industrial Co., Ltd. on March 05, 2021. The current certification is valid through December 31, 2022.

How is this Zhejiang Dianfeng Industrial Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81648000101. 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)
81648-001-01
11-Digit CMS (5-4-2)
81648-0001-01

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