Biofreeze Day And Overnight Kit
NDC Package 59316-832-94

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Biofreeze Day And Overnight (menthol) kits is ■ adults and children 12 years of age and older: Clean and dry affected area, pop apart and partially peel back protective film and apply exposed patch to site of pain. This formulation utilizes a kit delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 59316-832 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
59316-832-94
Package Description
1 KIT in 1 KIT * 1 PATCH in 1 POUCH (59316-992-07) / 9 g in 1 PATCH * 6 g in 1 PATCH (59316-005-03)
Product Code
59316-832
11-Digit Billing Format
59316083294
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Biofreeze Day And Overnight
Non-Proprietary Name
Menthol
Dosage Form
Kit - A packaged collection of related material.
Usage Information
■ adults and children 12 years of age and older: Clean and dry affected area, pop apart and partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing the patch to skin and leave in place for up to 8 hours. Use on affected area not more than 3 to 4 times daily. ■ children under 12 years of age: consult a physician ■wash hands after use with cool water

Regulatory & Marketing

Labeler Name
Reckitt Benckiser Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-22-2023
Listing Expiration
12-31-2027
Exclude Flag
N
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 59316-832-94 identifies a specific commercial package of 1 kit in 1 kit * 1 patch in 1 pouch (59316-992-07) / 9 g in 1 patch * 6 g in 1 patch (59316-005-03) of Biofreeze Day And Overnight, a human over the counter drug labeled by Reckitt Benckiser Llc. This kit is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Reckitt Benckiser Llc on May 22, 2023. The current certification is valid through December 31, 2027.

How is this Reckitt Benckiser Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59316083294. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. 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)
59316-832-94
11-Digit CMS (5-4-2)
59316-0832-94

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