Caraderma
NDC Package 51130-333-12

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.

Caraderma is cleanse the skin thoroughly before applying.Cover the entire affected area with a thin layer one to three times daily.Because excessive drying may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.If going outside, use a sunscreen.Allow CaraDerma® to dry before applying sunscreen.If irritation or sensitivity develops, discontinue use and consult a doctor. Marketed by A Refreshing Discovery, Inc., this product is identified by NDC 51130-333 and is authorized under FDA application part333D.

Identification & Billing

NDC Package Code
51130-333-12
Package Description
1 JAR in 1 CARTON / 15 g in 1 JAR
Product Code
51130-333
11-Digit Billing Format
51130033312
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Caraderma
Dosage Form
-
Usage Information
Cleanse the skin thoroughly before applying.Cover the entire affected area with a thin layer one to three times daily.Because excessive drying may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.If going outside, use a sunscreen.Allow CaraDerma® to dry before applying sunscreen.If irritation or sensitivity develops, discontinue use and consult a doctor.

Regulatory & Marketing

Labeler Name
A Refreshing Discovery, Inc.
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
09-02-2010
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 51130-333-12 identifies a specific commercial package of 1 jar in 1 carton / 15 g in 1 jar of Caraderma, labeled by A Refreshing Discovery, Inc.. 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 A Refreshing Discovery, Inc. on September 02, 2010. The current certification is valid through December 31, 2017.

How is this A Refreshing Discovery, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51130033312. 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)
51130-333-12
11-Digit CMS (5-4-2)
51130-0333-12

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