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  5. NDC Package Code: 58552-148-04 Childrens Giltuss D

NDC Package 58552-148-04 Childrens Giltuss D

Syrup 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:
58552-148-04
Package Description:
1 BOTTLE in 1 CARTON / 1 SYRUP in 1 BOTTLE
Product Code:
58552-148
Proprietary Name:
Childrens Giltuss D
Non-Proprietary Name:
Childrens Giltuss D
Substance Name:
Chlorpheniramine Maleate; Phenylephrine Hydrochloride
Usage Information:
UsesTemporarily relieves these Symptoms due to hay fever (allergic rhinitis) or other upper-respiratory allergies:runny noseSneezingItchy, watery eyesnasal congestionitching of the nose or throatsinus congestion and pressure
11-Digit NDC Billing Format:
58552014804
Product Type:
Human Otc Drug
Labeler Name:
Gil Pharmaceutical Corp
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):
  • CHLORPHENIRAMINE MALEATE 1.75 mg/1
  • PHENYLEPHRINE HYDROCHLORIDE 5 mg/1
    • Pharmacologic Class(es):
  • Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-11-2024
    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.

    Frequently Asked Questions

    What is NDC 58552-148-04?

    The NDC Packaged Code 58552-148-04 is assigned to a package of 1 bottle in 1 carton / 1 syrup in 1 bottle of Childrens Giltuss D, a human over the counter drug labeled by Gil Pharmaceutical Corp. The product's dosage form is syrup and is administered via oral form.

    Is NDC 58552-148 included in the NDC Directory?

    Yes, Childrens Giltuss D with product code 58552-148 is active and included in the NDC Directory. The product was first marketed by Gil Pharmaceutical Corp on April 11, 2024 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 58552-148-04?

    The 11-digit format is 58552014804. 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
    5-3-258552-148-045-4-258552-0148-04