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  5. NDC Package Code: 56062-741-25 Allergy Relief

NDC Package 56062-741-25 Allergy Relief

Cetirizine Hcl Capsule Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
56062-741-25
Package Description:
1 BOTTLE in 1 BOX / 25 CAPSULE in 1 BOTTLE
Product Code:
56062-741
Proprietary Name:
Allergy Relief
Non-Proprietary Name:
Cetirizine Hcl
Substance Name:
Cetirizine Hydrochloride
Usage Information:
Diphenhydramine is an antihistamine used to relieve symptoms of allergy, hay fever, and the common cold. These symptoms include rash, itching, watery eyes, itchy eyes/nose/throat, cough, runny nose, and sneezing. It is also used to prevent and treat nausea, vomiting and dizziness caused by motion sickness. Diphenhydramine can also be used to help you relax and fall asleep. This medication works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Its drying effects on such symptoms as watery eyes and runny nose are caused by blocking another natural substance made by your body (acetylcholine). Cough-and-cold products have not been shown to be safe or effective in children younger than 6 years. Therefore, do not use this product to treat cold symptoms in children younger than 6 years unless specifically directed by the doctor. Some products (such as long-acting tablets/capsules) are not recommended for use in children younger than 12 years. Ask your doctor or pharmacist for more details about using your product safely. These products do not cure or shorten the length of the common cold and may cause serious side effects. To decrease the risk for serious side effects, carefully follow all dosage directions. Do not use this product to make a child sleepy. Do not give other cough-and-cold medication that might contain the same or similar ingredients (see also Drug Interactions section). Ask the doctor or pharmacist about other ways to relieve cough and cold symptoms (such as drinking enough fluids, using a humidifier or saline nose drops/spray).
11-Digit NDC Billing Format:
56062074125
NDC to RxNorm Crosswalk:
  • RxCUI: 1014675 - cetirizine HCl 10 MG 24HR Oral Capsule
  • RxCUI: 1014675 - cetirizine hydrochloride 10 MG Oral Capsule
  • RxCUI: 1014675 - cetirizine HCl 10 MG 24 HR Oral Capsule
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Publix Supermarkets, Inc.
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • CETIRIZINE HYDROCHLORIDE 10 mg/1
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA207235
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-28-2019
    End Marketing Date:
    02-28-2025
    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 56062-741-25?

    The NDC Packaged Code 56062-741-25 is assigned to a package of 1 bottle in 1 box / 25 capsule in 1 bottle of Allergy Relief, a human over the counter drug labeled by Publix Supermarkets, Inc.. The product's dosage form is capsule and is administered via oral form.

    Is NDC 56062-741 included in the NDC Directory?

    Yes, Allergy Relief with product code 56062-741 is active and included in the NDC Directory. The product was first marketed by Publix Supermarkets, Inc. on February 28, 2019.

    What is the 11-digit format for NDC 56062-741-25?

    The 11-digit format is 56062074125. 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 5-3-2 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
    5-3-256062-741-255-4-256062-0741-25