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  5. NDC Package Code: 73238-002-01 Skineez

NDC Package 73238-002-01 Skineez

Menthol,Retinol Cloth Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
73238-002-01
Package Description:
4.66 g in 1 PACKET
Product Code:
73238-002
Proprietary Name:
Skineez
Non-Proprietary Name:
Menthol, Retinol
Substance Name:
Menthol; Vitamin A
Usage Information:
• After 10 washes, in order to continue receiving the hydrating benefits, the garment will need to be re-infused with SKINEEZ® GARMENT SPRAY® (not included). • Machine wash the garment in cold water with like colors, then while wet turn it inside out and spray the areas of the garment that you wish to re-infuse. • Tumble dry low or lay flat to dry. • Do not Bleach.
11-Digit NDC Billing Format:
73238000201
Product Type:
Human Otc Drug
Labeler Name:
Cause For Change Llc
Dosage Form:
Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.
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 .05 g/4.66g
  • VITAMIN A .01 g/4.66g
    • Pharmacologic Class(es):
  • Vitamin A - [CS]
  • Vitamin A - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M016
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    09-27-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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 73238-002-01?

    The NDC Packaged Code 73238-002-01 is assigned to a package of 4.66 g in 1 packet of Skineez, a human over the counter drug labeled by Cause For Change Llc. The product's dosage form is cloth and is administered via topical form.

    Is NDC 73238-002 included in the NDC Directory?

    Yes, Skineez with product code 73238-002 is active and included in the NDC Directory. The product was first marketed by Cause For Change Llc on September 27, 2023 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 11-digit format for NDC 73238-002-01?

    The 11-digit format is 73238000201. 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 5-3-2 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
    5-3-273238-002-015-4-273238-0002-01