Kenaf Wet Wipe Kids Liquid
NDC Package 72944-0002-1

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

Package Information

Kenaf Wet Wipe Kids (allantoin) liquids is apply to skin and wipe. This formulation utilizes a liquid delivery system. Marketed by Medicell Bio Co., Ltd., this product is identified by NDC 72944-0002.

Identification & Billing

NDC Package Code
72944-0002-1
Package Description
190 g in 1 POUCH
Product Code
72944-0002
11-Digit Billing Format
72944000201

Clinical Specifications

Proprietary Name
Kenaf Wet Wipe Kids
Non-Proprietary Name
Allantoin
Substance Name
Allantoin
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
ALLANTOIN .05 g/100g
Usage Information
Apply to skin and wipe

Regulatory & Marketing

Labeler Name
Medicell Bio Co., Ltd.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
04-09-2017
Listing Expiration
12-31-2026
Exclude Flag
N
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 72944-0002-1 identifies a specific commercial package of 190 g in 1 pouch of Kenaf Wet Wipe Kids, a human over the counter drug labeled by Medicell Bio Co., Ltd.. This liquid is formulated for topical use and contains allantoin 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 Medicell Bio Co., Ltd. on April 09, 2017. The current certification is valid through December 31, 2026.

How is this Medicell Bio Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72944000201. 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 (5-4-1)
72944-0002-1
11-Digit CMS (5-4-2)
72944-0002-01

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