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  5. NDC Package Code: 72988-0033-1 Nocold-s

NDC Package 72988-0033-1 Nocold-s

Acetaminophen,Chlorpheniramine Maleate Liquid 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:
72988-0033-1
Package Description:
20 mL in 1 BOTTLE
Product Code:
72988-0033
Proprietary Name:
Nocold-s
Non-Proprietary Name:
Acetaminophen, Chlorpheniramine Maleate
Substance Name:
Acetaminophen; Chlorpheniramine Maleate
Usage Information:
■ Adult and children 16 years and over: take 1 bottle (20ml) per session 3 times per day after meal
11-Digit NDC Billing Format:
72988003301
NDC to RxNorm Crosswalk:
  • RxCUI: 2645106 - acetaminophen 200 MG / chlorpheniramine maleate 2.5 MG in 20 mL Oral Solution
  • RxCUI: 2645106 - acetaminophen 10 MG/ML / chlorpheniramine maleate 0.125 MG/ML Oral Solution
  • RxCUI: 2645106 - acetaminophen 200 MG / chlorpheniramine maleate 2.5 MG per 20 ML Oral Solution
  • RxCUI: 2645106 - APAP 10 MG/ML / chlorpheniramine maleate 0.125 MG/ML Oral Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Lydia Co., Ltd.
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 200 mg/20mL
  • CHLORPHENIRAMINE MALEATE 2.5 mg/20mL
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    01-23-2023
    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 72988-0033-1?

    The NDC Packaged Code 72988-0033-1 is assigned to a package of 20 ml in 1 bottle of Nocold-s, a human over the counter drug labeled by Lydia Co., Ltd.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 72988-0033 included in the NDC Directory?

    Yes, Nocold-s with product code 72988-0033 is active and included in the NDC Directory. The product was first marketed by Lydia Co., Ltd. on January 23, 2023 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 72988-0033-1?

    The 11-digit format is 72988003301. 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
    5-4-172988-0033-15-4-272988-0033-01