Extra Strength Wal-dryl Itch Relief Spray
NDC Package 0363-2177-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Extra Strength Wal-dryl Itch Relief (diphenhydramine, zinc acetate) sprays is uses:Temporarily relieves pain and itching associated with: insect bites, minor burns and cuts, sunburn, scrapes, minor skin irritations, rashes due to poison ivy, oak and sumac, dries the oozing and weeping of poison ivy, poison oak and poison sumac. This formulation utilizes a spray delivery system. Marketed by Walgreen Co, this product is identified by NDC 0363-2177 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
0363-2177-00
Package Description
88 mL in 1 BOTTLE, SPRAY
Product Code
0363-2177
11-Digit Billing Format
00363217700
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]

Clinical Specifications

Proprietary Name
Extra Strength Wal-dryl Itch Relief
Non-Proprietary Name
Diphenhydramine, Zinc Acetate
Substance Name
Diphenhydramine Hydrochloride; Zinc Acetate
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
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)
Pharmacologic Class
Usage Information
Uses:Temporarily relieves pain and itching associated with: insect bites, minor burns and cuts, sunburn, scrapes, minor skin irritations, rashes due to poison ivy, oak and sumac, dries the oozing and weeping of poison ivy, poison oak and poison sumac.

Regulatory & Marketing

Labeler Name
Walgreen Co
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-03-2011
Listing Expiration
12-31-2026
Exclude Flag
N
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 0363-2177-00 identifies a specific commercial package of 88 ml in 1 bottle, spray of Extra Strength Wal-dryl Itch Relief, a human over the counter drug labeled by Walgreen Co. This spray is formulated for topical use and contains diphenhydramine hydrochloride; zinc acetate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Walgreen Co on January 03, 2011. The current certification is valid through December 31, 2026.

How is this Walgreen Co product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363217700. 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 (4-4-2)
0363-2177-00
11-Digit CMS (5-4-2)
00363-2177-00

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