Alcohol Prep
NDC Package 68016-012-90

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 Prep is stop use and ask a doctor if:Irritation or redness developscondition persists for more than 72 hoursCleansing of an injection site. Marketed by Chain Drug Consortium, Llc, this product is identified by NDC 68016-012 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
68016-012-90
Package Description
10 BOX in 1 CASE / 100 SWAB in 1 BOX
Product Code
68016-012
11-Digit Billing Format
68016001290
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
10 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Alcohol Prep
Dosage Form
-
Usage Information
Stop use and ask a doctor if:Irritation or redness developscondition persists for more than 72 hoursCleansing of an injection site

Regulatory & Marketing

Labeler Name
Chain Drug Consortium, Llc
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
04-21-2011
Listing Expiration
12-31-2018
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 68016-012-90 identifies a specific commercial package of 10 box in 1 case / 100 swab in 1 box of Alcohol Prep, labeled by Chain Drug Consortium, Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 10 billable units per package. 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 Chain Drug Consortium, Llc on April 21, 2011. The current certification is valid through December 31, 2018.

How is this Chain Drug Consortium, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68016001290. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 10 total billable units per package. 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)
68016-012-90
11-Digit CMS (5-4-2)
68016-0012-90

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