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  5. NDC Package Code: 70359-4106-1 Poxiezzz

NDC Package 70359-4106-1 Poxiezzz

View Billable Units, 11-Digit Format, RxNorm

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.

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:
70359-4106-1
Package Description:
1 BOTTLE, SPRAY in 1 CARTON / 50 g in 1 BOTTLE, SPRAY
Product Code:
70359-4106
Proprietary Name:
Poxiezzz
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.
11-Digit NDC Billing Format:
70359410601
NDC to RxNorm Crosswalk:
  • RxCUI: 1733853 - menthol 1 % / zinc oxide 4 % Topical Spray
  • RxCUI: 1733853 - menthol 10 MG/ML / zinc oxide 40 MG/ML Topical Spray
  • RxCUI: 1733853 - Menthol 10 MG/ML / ZNO 40 MG/ML Topical Spray
    • Labeler Name:
    Fortunique B.v.
    Sample Package:
    No
    Start Marketing Date:
    01-21-2016
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    Code Structure:

    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 70359-4106-1?

    The NDC Packaged Code 70359-4106-1 is assigned to a package of 1 bottle, spray in 1 carton / 50 g in 1 bottle, spray of Poxiezzz, labeled by Fortunique B.v.. The product's dosage form is and is administered via form.

    Is NDC 70359-4106 included in the NDC Directory?

    No, Poxiezzz with product code 70359-4106 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Fortunique B.v. on January 21, 2016 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70359-4106-1?

    The 11-digit format is 70359410601. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-170359-4106-15-4-270359-4106-01