Rite Aid Anti-itch Gel
NDC Package 11822-1070-3

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

Package Information

Rite Aid Anti-itch (diphenhydramine hcl 2%) gel is for the temporary relief of pain and itching associated with insect bites, minor burns, sunburn, minor cuts, scrapes, minor skin irritations, and rashes due to poison ivy, oak, and sumac. This formulation utilizes a gel delivery system. Marketed by Rite Aid, this product is identified by NDC 11822-1070 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
11822-1070-3
Package Description
103 mL in 1 TUBE
Product Code
11822-1070
11-Digit Billing Format
11822107003
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Rite Aid Anti-itch
Non-Proprietary Name
Diphenhydramine Hcl 2%
Substance Name
Diphenhydramine Hydrochloride
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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)
DIPHENHYDRAMINE HYDROCHLORIDE 2 g/100mL
Pharmacologic Class
Usage Information
For the temporary relief of pain and itching associated with insect bites, minor burns, sunburn, minor cuts, scrapes, minor skin irritations, and rashes due to poison ivy, oak, and sumac.

Regulatory & Marketing

Labeler Name
Rite Aid
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-31-2021
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 11822-1070-3 identifies a specific commercial package of 103 ml in 1 tube of Rite Aid Anti-itch, a human over the counter drug labeled by Rite Aid. This gel is formulated for topical use and contains diphenhydramine hydrochloride 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 Rite Aid on March 31, 2021. The current certification is valid through December 31, 2026.

How is this Rite Aid product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11822107003. 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 (5-4-1)
11822-1070-3
11-Digit CMS (5-4-2)
11822-1070-03

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