Zims Max Freeze Liquid
NDC Package 54273-009-01

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

Package Information

Zims Max Freeze (menthol, unspecified form) liquids is adults and children 12 years of age and over:apply to affected area not more than 4 times dailyChildren under 12 years of age:consult a doctor. This formulation utilizes a liquid delivery system. Marketed by Kobayashi Healthcare International, Inc., this product is identified by NDC 54273-009 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
54273-009-01
Package Description
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 89 mL in 1 BOTTLE, WITH APPLICATOR
Product Code
54273-009
11-Digit Billing Format
54273000901
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Zims Max Freeze Pro Formula
Non-Proprietary Name
Menthol, Unspecified Form
Substance Name
Menthol, Unspecified Form
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
MENTHOL, UNSPECIFIED FORM 160 mg/mL
Usage Information
Adults and children 12 years of age and over:apply to affected area not more than 4 times dailyChildren under 12 years of age:consult a doctor

Regulatory & Marketing

Labeler Name
Kobayashi Healthcare International, Inc.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-20-2018
Listing Expiration
12-31-2026
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 54273-009-01 identifies a specific commercial package of 1 bottle, with applicator in 1 carton / 89 ml in 1 bottle, with applicator of Zims Max Freeze Pro Formula, a human over the counter drug labeled by Kobayashi Healthcare International, Inc.. This liquid is formulated for topical use and contains menthol, unspecified form 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 Kobayashi Healthcare International, Inc. on August 20, 2018. The current certification is valid through December 31, 2026.

How is this Kobayashi Healthcare International, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54273000901. 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)
54273-009-01
11-Digit CMS (5-4-2)
54273-0009-01

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