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  5. NDC Package Code: 72663-580-02 Anti-itch

NDC Package 72663-580-02 Anti-itch

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:
72663-580-02
Package Description:
.9 mL in 1 POUCH
Product Code:
72663-580
Proprietary Name:
Anti-itch
Usage Information:
This medication is used to temporarily relieve itching and pain caused by minor burns/cuts/scrapes, sunburn, insect bites, minor skin irritations, or rashes from poison ivy, poison oak, or poison sumac. Diphenhydramine belongs to a class of drugs known as antihistamines. It works by blocking the effects of a certain natural substance (histamine) that causes itching. This product may also contain other ingredients (skin protectants such as allantoin, zinc acetate) that may help relieve symptoms such as dry skin, weeping, or oozing. Read the product package for more information. Depending on the brand and the form of diphenhydramine skin product you are using, the package information may state that its use is not recommended in children younger than 2, 6, or 12 years unless directed by the doctor. If you are self-treating with this medication, it is important to read the package instructions carefully before you start using this product to be sure it is right for you. (See also Precautions section.)
11-Digit NDC Billing Format:
72663058002
Labeler Name:
Welly Health Pcb
Sample Package:
No
Start Marketing Date:
02-25-2019
Listing Expiration Date:
12-31-2021
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 72663-580-02?

The NDC Packaged Code 72663-580-02 is assigned to a package of .9 ml in 1 pouch of Anti-itch, labeled by Welly Health Pcb. The product's dosage form is and is administered via form.

Is NDC 72663-580 included in the NDC Directory?

No, Anti-itch with product code 72663-580 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Welly Health Pcb on February 25, 2019 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72663-580-02?

The 11-digit format is 72663058002. 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
5-3-272663-580-025-4-272663-0580-02