NDC Package 50090-6358-0 Biofreeze Roll-on

Menthol Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

50090-6358-0

Package Description:

74 mL in 1 BOTTLE

Product Code:

50090-6358

Proprietary Name:

Biofreeze Roll-on

Non-Proprietary Name:

Menthol

Substance Name:

Menthol

Usage Information:

Adults and children 2 years of age and older: rub a thin film over affected area not more than 3 to 4 times dailychildren under 2 years of age: consult a physicianwash hands after use with cool water

11-Digit NDC Billing Format:

50090635800

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

74 ML

NDC to RxNorm Crosswalk:

RxCUI: 1111683 - BIOFREEZE 4 % Topical Gel

RxCUI: 1111683 - menthol 0.04 MG/MG Topical Gel [Biofreeze]

RxCUI: 1111683 - Biofreeze 0.04 MG/MG Topical Gel

RxCUI: 1111683 - Biofreeze 4 % Topical Gel

RxCUI: 415974 - menthol 4 % Topical Gel

Product Type:

Human Otc Drug

Labeler Name:

A-s Medication Solutions

Dosage Form:

Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Administration Route(s):

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 40 mg/mL

Sample Package:

FDA Application Number:

M017

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

01-17-2013

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

50090 - A-s Medication Solutions
- 50090-6358 - Biofreeze Roll-on
  - 50090-6358-0 - 74 mL in 1 BOTTLE

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 disclaimer below.

Frequently Asked Questions

What is NDC 50090-6358-0?

The NDC Packaged Code 50090-6358-0 is assigned to a package of 74 ml in 1 bottle of Biofreeze Roll-on, a human over the counter drug labeled by A-s Medication Solutions. The product's dosage form is gel and is administered via topical form.This product is billed per "ML" milliliter and contains an estimated amount of 74 billable units per package.

Is NDC 50090-6358 included in the NDC Directory?

Yes, Biofreeze Roll-on with product code 50090-6358 is active and included in the NDC Directory. The product was first marketed by A-s Medication Solutions on January 17, 2013 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 50090-6358-0?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 74.

What is the 11-digit format for NDC 50090-6358-0?

The 11-digit format is 50090635800. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	50090-6358-0	5-4-2	50090-6358-00

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