Revitol
NDC Package 24488-004-20

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.

Revitol is cleanse the skin thoroughly before applying  medicationCover the entire affected area with a thin layer one to three times a dayBecause excessive drying of the skin may occur, start with one application daily, then gradually increase to two ore three times daily if needed or as directed by a doctor. Marketed by Revitol Corporation, this product is identified by NDC 24488-004 and is authorized under FDA application part333D.

Identification & Billing

NDC Package Code
24488-004-20
Package Description
59 mL in 1 JAR
Product Code
24488-004
11-Digit Billing Format
24488000420
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Revitol Acne Treatment
Dosage Form
-
Usage Information
Cleanse the skin thoroughly before applying  medicationCover the entire affected area with a thin layer one to three times a dayBecause excessive drying of the skin may occur, start with one application daily, then gradually increase to two ore three times daily if needed or as directed by a doctor. If bothersome drying or peeling occurs, reduce application to once a day or every other day.If going outside, use a sunscreen. Allow Acne Treatment Cream to dry, then follow directions in sunscreen labeling if sensitivity develops, discontinue use of both products and ask a doctor.

Regulatory & Marketing

Labeler Name
Revitol Corporation
FDA Application #
part333D
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
04-14-2011
Listing Expiration
12-31-2017
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 24488-004-20 identifies a specific commercial package of 59 ml in 1 jar of Revitol Acne Treatment, labeled by Revitol Corporation. 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 Revitol Corporation on April 14, 2011. The current certification is valid through December 31, 2017.

How is this Revitol Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24488000420. 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)
24488-004-20
11-Digit CMS (5-4-2)
24488-0004-20

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