1. Home
  2. Labeler Index
  3. Rite Aid Corporation
  4. 11822-4202
  5. NDC Package Code: 11822-4202-0 Eye Itch Relief

NDC Package 11822-4202-0 Eye Itch Relief

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:
11822-4202-0
Package Description:
2 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Product Code:
11822-4202
Proprietary Name:
Eye Itch Relief
Usage Information:
This medication is used to prevent and treat itching of the eyes caused by allergies (allergic/seasonal conjunctivitis). Ketotifen is an antihistamine for the eye that treats allergic symptoms by blocking a certain natural substance (histamine). It is also a mast cell stabilizer that prevents allergic reactions by reducing the release of natural substances that cause an allergic reaction.
11-Digit NDC Billing Format:
11822420200
NDC to RxNorm Crosswalk:
  • RxCUI: 311237 - ketotifen 0.025 % Ophthalmic Solution
  • RxCUI: 311237 - ketotifen 0.25 MG/ML Ophthalmic Solution
  • RxCUI: 311237 - ketotifen 0.025 % (as ketotifen fumarate 0.035 % ) Ophthalmic Solution
  • RxCUI: 311237 - ketotifen 0.25 MG/ML (as ketotifen fumarate 0.35 MG/ML) Ophthalmic Solution
    • Labeler Name:
    Rite Aid Corporation
    Sample Package:
    No
    Start Marketing Date:
    12-06-2013
    Listing Expiration Date:
    12-31-2023
    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 11822-4202-0?

    The NDC Packaged Code 11822-4202-0 is assigned to a package of 2 bottle, dropper in 1 carton / 5 ml in 1 bottle, dropper of Eye Itch Relief, labeled by Rite Aid Corporation. The product's dosage form is and is administered via form.

    Is NDC 11822-4202 included in the NDC Directory?

    No, Eye Itch Relief with product code 11822-4202 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rite Aid Corporation on December 06, 2013 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 11822-4202-0?

    The 11-digit format is 11822420200. 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 5-4-1 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
    5-4-111822-4202-05-4-211822-4202-00