NDC Package 24286-1551-4 Bactimicina Childrens Cough And Cold

Chlorpheniramine Maleate,Dextromethorphan Hydrobromide Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

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:
24286-1551-4
Package Description:
1 BOTTLE in 1 BOX / 118 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Bactimicina Childrens Cough And Cold
Non-Proprietary Name:
Chlorpheniramine Maleate, Dextromethorphan Hydrobromide
Substance Name:
Chlorpheniramine Maleate; Dextromethorphan Hydrobromide
Usage Information:
Do not take more than 4 doses in any 24-hour periodAge (years) DoseUnder 6do not use6-112 teaspoons (10 mL) every 6 hours12 and over4 teaspoons (20 mL) every 6 hours
11-Digit NDC Billing Format:
24286155104
NDC to RxNorm Crosswalk:
  • RxCUI: 1111440 - chlorpheniramine maleate 1 MG / dextromethorphan HBr 7.5 MG in 5 mL Oral Solution
  • RxCUI: 1111440 - chlorpheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML Oral Solution
  • RxCUI: 1111440 - chlorpheniramine maleate 1 MG / dextromethorphan hydrobromide 7.5 MG per 5 ML Oral Solution
  • RxCUI: 1111440 - chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG per 10 ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Dlc Laboratories, Inc.
    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.
  • 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:
    10-23-2009
    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 24286-1551-4?

    The NDC Packaged Code 24286-1551-4 is assigned to a package of 1 bottle in 1 box / 118 ml in 1 bottle of Bactimicina Childrens Cough And Cold, a human over the counter drug labeled by Dlc Laboratories, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 24286-1551 included in the NDC Directory?

    Yes, Bactimicina Childrens Cough And Cold with product code 24286-1551 is active and included in the NDC Directory. The product was first marketed by Dlc Laboratories, Inc. on October 23, 2009 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 24286-1551-4?

    The 11-digit format is 24286155104. 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
    5-4-124286-1551-45-4-224286-1551-04