Multivitamin Bodyblock
NDC Package 21839-101-25

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.

Multivitamin Bodyblock is a . Marketed by Gordon Laboratories, Inc, this product is identified by NDC 21839-101 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
21839-101-25
Package Description
1 TUBE in 1 BOX / 125 mL in 1 TUBE
Product Code
21839-101
11-Digit Billing Format
21839010125

Clinical Specifications

Proprietary Name
Multivitamin Bodyblock Spf 20
Dosage Form
-

Regulatory & Marketing

Labeler Name
Gordon Laboratories, Inc
FDA Application #
part352
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
11-01-2005
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 21839-101-25 identifies a specific commercial package of 1 tube in 1 box / 125 ml in 1 tube of Multivitamin Bodyblock Spf 20, labeled by Gordon 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 Gordon Laboratories, Inc on November 01, 2005. The current certification is valid through December 31, 2017.

How is this Gordon Laboratories, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 21839010125. 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)
21839-101-25
11-Digit CMS (5-4-2)
21839-0101-25

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