Rite Aid Cala Itch Relief Spray
NDC Package 11822-3101-3

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

Package Information

Rite Aid Cala Itch Relief (pramoxine hcl 1%, zinc acetate 0.1%) sprays 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 spray delivery system. Marketed by Rite Aid, this product is identified by NDC 11822-3101 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
11822-3101-3
Package Description
85 g in 1 CAN
Product Code
11822-3101
11-Digit Billing Format
11822310103
RxNorm Crosswalk
  • RxCUI: 1294033 - pramoxine HCl 1 % / zinc acetate 0.1 % Topical Spray
  • RxCUI: 1294033 - pramoxine hydrochloride 10 MG/ML / zinc acetate 1 MG/ML Topical Spray

Clinical Specifications

Proprietary Name
Rite Aid Cala Itch Relief
Non-Proprietary Name
Pramoxine Hcl 1%, Zinc Acetate 0.1%
Substance Name
Pramoxine 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
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. Dries the oozing and weeping of 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 11822-3101-3 identifies a specific commercial package of 85 g in 1 can of Rite Aid Cala Itch Relief, a human over the counter drug labeled by Rite Aid. This spray is formulated for topical use and contains pramoxine 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 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: 11822310103. 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)
11822-3101-3
11-Digit CMS (5-4-2)
11822-3101-03

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