Poxiezzz
NDC Package 70359-4106-1

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.

Poxiezzz is not suitable for children under 2 years of age. Marketed by Fortunique B.v., this product is identified by NDC 70359-4106 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
70359-4106-1
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 50 g in 1 BOTTLE, SPRAY
Product Code
70359-4106
11-Digit Billing Format
70359410601
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Poxiezzz
Dosage Form
-
Usage Information
Not suitable for children under 2 years of age. Adults and children 2 years of age and older: Apply to affected area no more than 2 to 3 times daily. Shake well before use. Make sure the skin is clean and dry before spraying. Use a sweeping movement to spray-on the cream in a thin and uniform layer directly onto the affected skin. Use a spraying distance of approximately 2 to 3 inches. It is not necessary to rub the cream. When the skin is very sensitive, it is advised not to touch the skin too frequently.

Regulatory & Marketing

Labeler Name
Fortunique B.v.
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-21-2016
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 70359-4106-1 identifies a specific commercial package of 1 bottle, spray in 1 carton / 50 g in 1 bottle, spray of Poxiezzz, labeled by Fortunique B.v.. 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 Fortunique B.v. on January 21, 2016. The current certification is valid through December 31, 2017.

How is this Fortunique B.v. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70359410601. 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)
70359-4106-1
11-Digit CMS (5-4-2)
70359-4106-01

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