NDC Package 50269-507-25 Tylenol Sinus Severe

Acetaminophen,Guaifenesin,Phenylephrine Hydrochloride Tablet, Coated 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:
50269-507-25
Package Description:
25 POUCH in 1 BOX / 2 TABLET, COATED in 1 POUCH
Product Code:
Proprietary Name:
Tylenol Sinus Severe
Non-Proprietary Name:
Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride
Substance Name:
Acetaminophen; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed (see overdose warning)adults and children 12 years and over take 2 caplets every 4 hoursswallow whole; do not crush, chew or dissolvedo not take more than 10 caplets in 24 hours children under 12 years ask a doctor
11-Digit NDC Billing Format:
50269050725
NDC to RxNorm Crosswalk:
  • RxCUI: 1243679 - acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1243679 - acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - APAP 325 MG / GG 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - APAP 325 MG / Guaifenesin 200 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Jc World Bell Wholesale Co., Inc.
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    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:
    09-20-2018
    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 50269-507-25?

    The NDC Packaged Code 50269-507-25 is assigned to a package of 25 pouch in 1 box / 2 tablet, coated in 1 pouch of Tylenol Sinus Severe, a human over the counter drug labeled by Jc World Bell Wholesale Co., Inc.. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 50269-507 included in the NDC Directory?

    Yes, Tylenol Sinus Severe with product code 50269-507 is active and included in the NDC Directory. The product was first marketed by Jc World Bell Wholesale Co., Inc. on September 20, 2018 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 50269-507-25?

    The 11-digit format is 50269050725. 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
    5-3-250269-507-255-4-250269-0507-25