NDC Package 0363-0295-16 Anti-itch Wal-dryl

Diphenhydramine Hcl,Zinc Acetate Spray Topical - View Billable Units, 11-Digit Format, RxNorm

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:
0363-0295-16
Package Description:
.059 L in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Anti-itch Wal-dryl
Non-Proprietary Name:
Diphenhydramine Hcl, Zinc Acetate
Substance Name:
Diphenhydramine Hydrochloride; Zinc Acetate
Usage Information:
•do note use more than directed•adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily•children under 2 years of age: ask a doctor
11-Digit NDC Billing Format:
00363029516
NDC to RxNorm Crosswalk:
  • RxCUI: 1053138 - diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Spray
  • RxCUI: 1053138 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray
  • RxCUI: 1053138 - diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Spray
  • RxCUI: 1053142 - WAL-DRYL 2 % / 0.1 % Topical Spray
  • RxCUI: 1053142 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray [Wal-Dryl]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walgreen's Co
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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.
  • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    07-08-2011
    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 0363-0295-16?

    The NDC Packaged Code 0363-0295-16 is assigned to a package of .059 l in 1 bottle, spray of Anti-itch Wal-dryl, a human over the counter drug labeled by Walgreen's Co. The product's dosage form is spray and is administered via topical form.

    Is NDC 0363-0295 included in the NDC Directory?

    Yes, Anti-itch Wal-dryl with product code 0363-0295 is active and included in the NDC Directory. The product was first marketed by Walgreen's Co on July 08, 2011 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 0363-0295-16?

    The 11-digit format is 00363029516. 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 4-4-2 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
    4-4-20363-0295-165-4-200363-0295-16