Techniblock Ultra Sunscreen
NDC Package 49672-100-01

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.

Techniblock Ultra Sunscreen is uses:Helps prevent SunburnHigher SPF gives more sunburn protection.Provides moderate protection against sunburn. Marketed by The Myles Group Llc, this product is identified by NDC 49672-100 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
49672-100-01
Package Description
125 mL in 1 PACKAGE
Product Code
49672-100
11-Digit Billing Format
49672010001

Clinical Specifications

Proprietary Name
Techniblock Ultra Sunscreen
Dosage Form
-
Usage Information
Uses:Helps prevent SunburnHigher SPF gives more sunburn protection.Provides moderate protection against sunburn.

Regulatory & Marketing

Labeler Name
The Myles Group Llc
FDA Application #
part352
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-05-2010
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 49672-100-01 identifies a specific commercial package of 125 ml in 1 package of Techniblock Ultra Sunscreen, labeled by The Myles Group Llc. 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 The Myles Group Llc on April 05, 2010. The current certification is valid through December 31, 2017.

How is this The Myles Group Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49672010001. 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)
49672-100-01
11-Digit CMS (5-4-2)
49672-0100-01

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