Nick Relief
NDC Package 57367-007-20

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.

Nick Relief is uses:Stops bleeding from minor nicks and cuts.No stinging or skin irritation.Helps to speed healing. Marketed by 220 Laboratories Inc, this product is identified by NDC 57367-007 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
57367-007-20
Package Description
1 APPLICATOR in 1 BLISTER PACK / 7 mL in 1 APPLICATOR (57367-007-07)
Product Code
57367-007
11-Digit Billing Format
57367000720

Clinical Specifications

Proprietary Name
Nick Relief
Dosage Form
-
Usage Information
Uses:Stops bleeding from minor nicks and cuts.No stinging or skin irritation.Helps to speed healing.

Regulatory & Marketing

Labeler Name
220 Laboratories Inc
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-27-1997
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 57367-007-20 identifies a specific commercial package of 1 applicator in 1 blister pack / 7 ml in 1 applicator (57367-007-07) of Nick Relief, labeled by 220 Laboratories 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 220 Laboratories Inc on November 27, 1997. The current certification is valid through December 31, 2017.

How is this 220 Laboratories Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 57367000720. 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)
57367-007-20
11-Digit CMS (5-4-2)
57367-0007-20

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