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  5. NDC Package Code: 29485-7318-2 Alka-seltzer Plus Cold And Flu

NDC Package 29485-7318-2 Alka-seltzer Plus Cold And Flu

Chlorpheniramine Maleate,Acetaminophen,Phenylephrine Hydrochloride,Dextromethorphan - 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:
29485-7318-2
Package Description:
25 PACKET in 1 BOX / 2 TABLET, EFFERVESCENT in 1 PACKET
Product Code:
29485-7318
Proprietary Name:
Alka-seltzer Plus Cold And Flu
Non-Proprietary Name:
Chlorpheniramine Maleate, Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide Tablet Tablet, Effervescent
Substance Name:
Acetaminophen; Chlorpheniramine Maleate; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Usage Information:
Directionsdo not take more than the recommended doseadults and children 12 years and over: take 2 tablets fully dissolved in 4 oz of water every 4 hours. Do not exceed 8 tablets in 24 hours or as directed by a doctor.children under 12 years: do not use
11-Digit NDC Billing Format:
29485731802
NDC to RxNorm Crosswalk:
  • RxCUI: 1536477 - acetaminophen 250 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Effervescent Oral Tablet
  • RxCUI: 1536477 - acetaminophen 250 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Effervescent Oral Tablet
  • RxCUI: 1536477 - APAP 250 MG / Chlorpheniramine Maleate 2 MG / Dextromethorphan Hydrobromide 10 MG / Phenylephrine Hydrochloride 5 MG Effervescent Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Lil' Drug Store Products, Inc.
    Dosage Form:
    Tablet, Effervescent - A solid dosage form containing mixtures of acids (e.g., citric acid, tartaric acid) and sodium bicarbonate, which release carbon dioxide when dissolved in water; it is intended to be dissolved or dispersed in water before administration.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 250 mg/1
  • CHLORPHENIRAMINE MALEATE 2 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE 10 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)
  • Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
  • Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
  • alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-23-2021
    End Marketing 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
    29485-7318-330 PACKET in 1 BOX / 2 TABLET, EFFERVESCENT in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 29485-7318-2?

    The NDC Packaged Code 29485-7318-2 is assigned to a package of 25 packet in 1 box / 2 tablet, effervescent in 1 packet of Alka-seltzer Plus Cold And Flu, a human over the counter drug labeled by Lil' Drug Store Products, Inc.. The product's dosage form is tablet, effervescent and is administered via oral form.

    Is NDC 29485-7318 included in the NDC Directory?

    Yes, Alka-seltzer Plus Cold And Flu with product code 29485-7318 is active and included in the NDC Directory. The product was first marketed by Lil' Drug Store Products, Inc. on December 23, 2021.

    What is the 11-digit format for NDC 29485-7318-2?

    The 11-digit format is 29485731802. 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
    5-4-129485-7318-25-4-229485-7318-02