Ltg Alcohol Prep Pads
NDC Package 81264-001-01

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.

Ltg Alcohol Prep Pads is use as part of your daily cleansing routineMay be covered with a sterile bandage. Marketed by Labotek Group Corp, this product is identified by NDC 81264-001 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
81264-001-01
Package Description
.7 mL in 1 POUCH
Product Code
81264-001
11-Digit Billing Format
81264000101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Ltg Alcohol Prep Pads
Dosage Form
-
Usage Information
Use as part of your daily cleansing routineMay be covered with a sterile bandage

Regulatory & Marketing

Labeler Name
Labotek Group Corp
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
12-18-2020
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 81264-001-01 identifies a specific commercial package of .7 ml in 1 pouch of Ltg Alcohol Prep Pads, labeled by Labotek Group Corp. 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 Labotek Group Corp on December 18, 2020. The current certification is valid through December 31, 2021.

How is this Labotek Group Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81264000101. 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)
81264-001-01
11-Digit CMS (5-4-2)
81264-0001-01

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