An Adc Face Up Special Program
NDC Package 69153-020-01

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.

An Adc Face Up Special Program is indications & usage:1. Marketed by An Co Ltd., this product is identified by NDC 69153-020 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
69153-020-01
Package Description
10 SOLUTION in 1 CARTON
Product Code
69153-020
11-Digit Billing Format
69153002001

Clinical Specifications

Proprietary Name
An Adc Face Up Special Program
Dosage Form
-
Usage Information
Indications & usage:1. Open the wine colored pack to the dotted line(please be careful not to spill any of the liquid inside)2. Open the small transparent vial and pour it into the pack (please be careful not to spill)3. Seal the wine colored pack tightly and shake it steadily but vigorously 10 or more times (after shaking adequately the contents should turn into gel).4. Apply the gel mixture all over the face with the included cosmetic brush.5. It may depend on the person, but the wait time is around 15-20 minutes (while waiting, fan your face lightly). Please refrain from moving or speaking as much as possible.6. The first few times the pack may pull very tightly and become discolored depending on the area (due to removing the wastes from inside the skin). The state of being pulled very taut does depend on the skin type, but there is nothing to worry about as the tightening is part of the process.7. After the pack is sufficiently dry, wash it off with warm water; wash twice with soap once again like step number 1 of 1.8. Dab away the excess moisture with a dry towel.

Regulatory & Marketing

Labeler Name
An Co Ltd.
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
08-01-2014
Listing Expiration
12-31-2019
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 69153-020-01 identifies a specific commercial package of 10 solution in 1 carton of An Adc Face Up Special Program, labeled by An 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 An Co Ltd. on August 01, 2014. The current certification is valid through December 31, 2019.

How is this An Co Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69153002001. 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)
69153-020-01
11-Digit CMS (5-4-2)
69153-0020-01

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