NDC Package 69729-143-72 Coldtac Plus

Acetaminophen,Phenylephrin Hydrochloride,Dextromethorphan Hydrobromide Tablet 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:
69729-143-72
Package Description:
72 POUCH in 1 PACKAGE / 2 TABLET in 1 POUCH (69729-143-02)
Product Code:
Proprietary Name:
Coldtac Plus
Non-Proprietary Name:
Acetaminophen, Phenylephrin Hydrochloride, Dextromethorphan Hydrobromide
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Adults and children 12 years of age and older: Take 2 tablets every 6 to 8 hours as needed, do not exceed 8 tablets in 24 hours, or as directed by a doctor. Children under 12 years, consult a doctor
11-Digit NDC Billing Format:
69729014372
NDC to RxNorm Crosswalk:
  • RxCUI: 1367204 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1367204 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1367204 - APAP 325 MG / dextromethorphan hydrobromide 15 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Opmx 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.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-05-2018
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    69729-143-066 POUCH in 1 PACKAGE / 2 TABLET in 1 POUCH (69729-143-02)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69729-143-72?

    The NDC Packaged Code 69729-143-72 is assigned to a package of 72 pouch in 1 package / 2 tablet in 1 pouch (69729-143-02) of Coldtac Plus, a human over the counter drug labeled by Opmx Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 69729-143 included in the NDC Directory?

    Yes, Coldtac Plus with product code 69729-143 is active and included in the NDC Directory. The product was first marketed by Opmx Llc on January 05, 2018 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 69729-143-72?

    The 11-digit format is 69729014372. 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
    5-3-269729-143-725-4-269729-0143-72