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  5. NDC Package Code: 11523-0008-1 Coricidin Hbp Cough And Cold

NDC Package 11523-0008-1 Coricidin Hbp Cough And Cold

Chlorpheniramine Maleate,Dextromethorphan Hydrochloride Tablet 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:
11523-0008-1
Package Description:
2 BLISTER PACK in 1 CARTON / 8 TABLET in 1 BLISTER PACK
Product Code:
11523-0008
Proprietary Name:
Coricidin Hbp Cough And Cold
Non-Proprietary Name:
Chlorpheniramine Maleate, Dextromethorphan Hydrochloride
Substance Name:
Chlorpheniramine Maleate; Dextromethorphan Hydrobromide
Usage Information:
This combination product is used for the temporary relief of cough, sneezing, or runny nose due to the common cold, hay fever or other upper respiratory allergies. This product contains a non-opioid cough suppressant (such as chlophedianol, dextromethorphan). It affects a certain part of the brain (cough center) to help you stop coughing. This product also contains an antihistamine (such as triprolidine, chlorpheniramine, doxylamine) that works by blocking the effects of a certain natural substance (histamine), which causes allergy symptoms. It also has a drying effect. Talk with your doctor before using this product for a chronic cough from smoking or a cough with too much/thick mucus. 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). Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the
11-Digit NDC Billing Format:
11523000801
NDC to RxNorm Crosswalk:
  • RxCUI: 1421985 - chlorpheniramine maleate 4 MG / dextromethorphan HBr 30 MG Oral Tablet
  • RxCUI: 1421985 - chlorpheniramine maleate 4 MG / dextromethorphan hydrobromide 30 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Bayer Healthcare Llc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • CHLORPHENIRAMINE MALEATE 4 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE 30 mg/1
    • Pharmacologic Class(es):
  • 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)
    • Sample Package:
    No
    FDA Application Number:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    10-23-2020
    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 11523-0008-1?

    The NDC Packaged Code 11523-0008-1 is assigned to a package of 2 blister pack in 1 carton / 8 tablet in 1 blister pack of Coricidin Hbp Cough And Cold, a human over the counter drug labeled by Bayer Healthcare Llc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 11523-0008 included in the NDC Directory?

    Yes, Coricidin Hbp Cough And Cold with product code 11523-0008 is active and included in the NDC Directory. The product was first marketed by Bayer Healthcare Llc. on October 23, 2020 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 11523-0008-1?

    The 11-digit format is 11523000801. 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
    5-4-111523-0008-15-4-211523-0008-01