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  5. NDC Package Code: 50580-730-06 Childrens Zyrtec

NDC Package 50580-730-06 Childrens Zyrtec

Cetirizine Hydrochloride Syrup Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50580-730-06
Package Description:
2 CARTON in 1 PACKAGE / 1 BOTTLE, PLASTIC in 1 CARTON / 118 mL in 1 BOTTLE, PLASTIC
Product Code:
50580-730
Proprietary Name:
Childrens Zyrtec
Non-Proprietary Name:
Cetirizine Hydrochloride
Substance Name:
Cetirizine Hydrochloride
Usage Information:
Use only with enclosed dosing cupfind right dose on chart belowmL = milliliteradults and children 6 years and over5 mL or 10 mL once daily depending upon severity of symptoms; do not take more than 10 mL in 24 hours.adults 65 years and over5 mL once daily; do not take more than 5 mL in 24 hours.children 2 to under 6 years of age2.5 mL once daily. If needed, dose can be increased to a maximum of 5 mL once daily or 2.5 mL every 12 hours. Do not give more than 5 mL in 24 hours.children under 2 years of ageask a doctorconsumers with liver or kidney diseaseask a doctor
11-Digit NDC Billing Format:
50580073006
NDC to RxNorm Crosswalk:
  • RxCUI: 1014673 - cetirizine HCl 5 MG in 5 mL Oral Solution
  • RxCUI: 1014673 - cetirizine hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1014673 - cetirizine HCl 1 MG/ML Oral Syrup
  • RxCUI: 1014673 - cetirizine HCl 5 MG per 5 ML Oral Solution
  • RxCUI: 1020021 - ZyrTEC 5 MG in 5 mL Oral Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    Dosage Form:
    Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • CETIRIZINE HYDROCHLORIDE 5 mg/5mL
    • 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:
    NDA022155
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-01-2009
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50580-730-011 BOTTLE, PLASTIC in 1 CARTON / 30 mL in 1 BOTTLE, PLASTIC
    50580-730-051 BOTTLE, PLASTIC in 1 CARTON / 118 mL in 1 BOTTLE, PLASTIC
    50580-730-173 TRAY in 1 PACKAGE / 1 BOTTLE in 1 TRAY / 118 mL in 1 BOTTLE
    50580-730-182 CARTON in 1 PACKAGE / 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
    50580-730-191 BOTTLE, PLASTIC in 1 CARTON / 240 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50580-730-06?

    The NDC Packaged Code 50580-730-06 is assigned to a package of 2 carton in 1 package / 1 bottle, plastic in 1 carton / 118 ml in 1 bottle, plastic of Childrens Zyrtec, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is syrup and is administered via oral form.

    Is NDC 50580-730 included in the NDC Directory?

    Yes, Childrens Zyrtec with product code 50580-730 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on June 01, 2009 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50580-730-06?

    The 11-digit format is 50580073006. 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
    5-3-250580-730-065-4-250580-0730-06