NDC Package 11822-1177-1 Childrens Allergy Nasal

Fluticasone Propionate Spray, Metered Nasal - 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:
11822-1177-1
Package Description:
1 BOTTLE in 1 CARTON / 72 SPRAY, METERED in 1 BOTTLE
Product Code:
Proprietary Name:
Childrens Allergy Nasal
Non-Proprietary Name:
Fluticasone Propionate
Substance Name:
Fluticasone Propionate
Usage Information:
Fluticasone is used to control and prevent symptoms (such as wheezing and shortness of breath) caused by asthma. Controlling symptoms of asthma helps you maintain your normal activities and decreases time lost from work or school. Fluticasone belongs to a class of drugs known as corticosteroids. It works by reducing swelling (inflammation) of the airways in the lungs to make breathing easier. This medication must be used regularly to be effective. It does not work right away and should not be used to relieve sudden asthma attacks. If an asthma attack occurs, use your quick-relief inhaler (such as albuterol, also called salbutamol in some countries) as prescribed.
11-Digit NDC Billing Format:
11822117701
NDC to RxNorm Crosswalk:
  • RxCUI: 1797907 - fluticasone propionate 50 MCG/ACTUAT Metered Dose Nasal Spray
  • RxCUI: 1797907 - fluticasone propionate 0.05 MG/ACTUAT Metered Dose Nasal Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Rite Aid Corporation
    Dosage Form:
    Spray, Metered - A non-pressurized dosage form consisting of valves which allow the dispensing of a specified quantity of spray upon each activation.
    Administration Route(s):
  • Nasal - Administration to the nose; administered by way of the nose.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA207957
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-22-2021
    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 11822-1177-1?

    The NDC Packaged Code 11822-1177-1 is assigned to a package of 1 bottle in 1 carton / 72 spray, metered in 1 bottle of Childrens Allergy Nasal, a human over the counter drug labeled by Rite Aid Corporation. The product's dosage form is spray, metered and is administered via nasal form.

    Is NDC 11822-1177 included in the NDC Directory?

    Yes, Childrens Allergy Nasal with product code 11822-1177 is active and included in the NDC Directory. The product was first marketed by Rite Aid Corporation on January 22, 2021 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 11822-1177-1?

    The 11-digit format is 11822117701. 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
    5-4-111822-1177-15-4-211822-1177-01