Anti Itch Balm
NDC Package 57285-100-02

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.

Anti Itch Balm is temporarily relieves itching associated with Insect bites, Eczema, Minor burn, Sunburn, Minor skin irritations, minor cuts, scrapes, atopic dermatitis. Marketed by Us Organic Group Corp, this product is identified by NDC 57285-100.

Identification & Billing

NDC Package Code
57285-100-02
Package Description
1 JAR in 1 CARTON / 28 g in 1 JAR (57285-100-01)
Product Code
57285-100
11-Digit Billing Format
57285010002
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Anti Itch Balm
Dosage Form
-
Usage Information
Temporarily relieves itching associated with Insect bites, Eczema, Minor burn, Sunburn, Minor skin irritations, minor cuts, scrapes, atopic dermatitis.

Regulatory & Marketing

Labeler Name
Us Organic Group Corp
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
03-29-2013
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 57285-100-02 identifies a specific commercial package of 1 jar in 1 carton / 28 g in 1 jar (57285-100-01) of Anti Itch Balm, labeled by Us Organic 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 Us Organic Group Corp on March 29, 2013. The current certification is valid through December 31, 2017.

How is this Us Organic Group Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 57285010002. 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)
57285-100-02
11-Digit CMS (5-4-2)
57285-0100-02

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