Onid Wipe Swab
NDC Package 71441-180-10

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

Package Information

Onid Wipe (ethanol) swabs is open packetremove and unfold wipewipe hands throughly for approximately 15 secondsdo not flush. This formulation utilizes a swab delivery system. Marketed by Onid Technology Corp, this product is identified by NDC 71441-180 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
71441-180-10
Package Description
.82 mL in 1 PACKET
Product Code
71441-180
11-Digit Billing Format
71441018010
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Onid Wipe
Non-Proprietary Name
Ethanol
Substance Name
Alcohol
Dosage Form
Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
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)
ALCOHOL 75 mL/100mL
Usage Information
Open packetremove and unfold wipewipe hands throughly for approximately 15 secondsdo not flush

Regulatory & Marketing

Labeler Name
Onid Technology Corp
Product Type
Human Otc Drug
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
06-28-2017
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 71441-180-10 identifies a specific commercial package of .82 ml in 1 packet of Onid Wipe, a human over the counter drug labeled by Onid Technology Corp. This swab 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 Onid Technology Corp on June 28, 2017. The current certification is valid through December 31, 2026.

How is this Onid Technology Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71441018010. 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)
71441-180-10
11-Digit CMS (5-4-2)
71441-0180-10

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