NDC Package 69729-222-06 Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl

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:
69729-222-06
Package Description:
3 POUCH in 1 CARTON / 2 TABLET in 1 POUCH
Product Code:
Proprietary Name:
Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl
Non-Proprietary Name:
Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl
Substance Name:
Acetaminophen; Chlorpheniramine Maleate; Phenylephrine Hydrochloride
Usage Information:
Temporarily relieves these symptoms of hay fever or other respiratory allergies:HeadacheNasal congestionSinus congestion & pressureRunny nose and sneezingMinor aches & painTemporarily relieves these additional symptoms of hay fever:itching of the nose or throatitchy, watery eyeshelps clear nasal passageshelps decongest sinus opening and passages
11-Digit NDC Billing Format:
69729022206
NDC to RxNorm Crosswalk:
  • RxCUI: 2463332 - acetaminophen 500 MG / chlorpheniramine maleate 4 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 2463332 - acetaminophen 500 MG / chlorpheniramine maleate 4 MG / phenylephrine hydrochloride 10 MG Oral Tablet
  • RxCUI: 2463332 - APAP 500 MG / chlorpheniramine maleate 4 MG / phenylephrine hydrochloride 10 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:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    08-26-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    69729-222-272 TABLET in 1 POUCH
    69729-222-3712 TABLET in 1 POUCH
    69729-222-38144 TABLET in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69729-222-06?

    The NDC Packaged Code 69729-222-06 is assigned to a package of 3 pouch in 1 carton / 2 tablet in 1 pouch of Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl, 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 69729-222 included in the NDC Directory?

    Yes, Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl with product code 69729-222 is active and included in the NDC Directory. The product was first marketed by Opmx Llc on August 26, 2019 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 69729-222-06?

    The 11-digit format is 69729022206. 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
    5-3-269729-222-065-4-269729-0222-06