Buttiezzz Daily
NDC Package 70359-4101-1

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.

Buttiezzz Daily is change wet or soiled diapers promptlyShake well before useMake sure the skin is clean and dry before use.Use a sweeping movement to spray-on the cream in a thin and uniform layer on the buttocksAllow to dryUse a spraying distance approximately 2 to 3 inchesApply Buttiezzz Daily liberally as often as necessary or at every diaper change. Marketed by Fortunique B.v., this product is identified by NDC 70359-4101 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
70359-4101-1
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 50 g in 1 BOTTLE, SPRAY
Product Code
70359-4101
11-Digit Billing Format
70359410101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Buttiezzz Daily
Dosage Form
-
Usage Information
Change wet or soiled diapers promptlyShake well before useMake sure the skin is clean and dry before use.Use a sweeping movement to spray-on the cream in a thin and uniform layer on the buttocksAllow to dryUse a spraying distance approximately 2 to 3 inchesApply Buttiezzz Daily liberally as often as necessary or at every diaper change

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
01-19-2016
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 70359-4101-1 identifies a specific commercial package of 1 bottle, spray in 1 carton / 50 g in 1 bottle, spray of Buttiezzz Daily, 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 19, 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: 70359410101. 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)
70359-4101-1
11-Digit CMS (5-4-2)
70359-4101-01

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