Osteo Bi-flex Roll-on
NDC Package 24737-1901-3

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Osteo Bi-flex Roll-on is directions: adults and children over 12 years: Roll directly onto affected area without the need to rub, massage or bandage. Marketed by The Nature's Bounty Company, this product is identified by NDC 24737-1901 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
24737-1901-3
Package Description
82 g in 1 BOTTLE, WITH APPLICATOR
Product Code
11-Digit Billing Format
24737190103
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Osteo Bi-flex Roll-on Extra Strength
Dosage Form
-
Usage Information
Directions: adults and children over 12 years: Roll directly onto affected area without the need to rub, massage or bandage. Repeat if necessary, but not more than 4 times daily.

Regulatory & Marketing

Labeler Name
The Nature's Bounty Company
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
03-31-2019
Listing Expiration
12-31-2020
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 24737-1901-3 identifies a specific commercial package of 82 g in 1 bottle, with applicator of Osteo Bi-flex Roll-on Extra Strength, labeled by The Nature's Bounty Company. 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 Nature's Bounty Company on March 31, 2019. The current certification is valid through December 31, 2020.

How is this The Nature's Bounty Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24737190103. 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 (5-4-1)
24737-1901-3
11-Digit CMS (5-4-2)
24737-1901-03

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