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  5. NDC Package Code: 49035-356-09 Day And Night Sinus

NDC Package 49035-356-09 Day And Night Sinus

Acetaminophen,Diphenhydramine Hcl,Guaifenesin,Phenylephrine Hcl Kit - 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:
49035-356-09
Package Description:
1 KIT in 1 CARTON * 10 TABLET, FILM COATED in 1 BLISTER PACK * 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
49035-356
Proprietary Name:
Day And Night Sinus
Non-Proprietary Name:
Acetaminophen, Diphenhydramine Hcl, Guaifenesin, Phenylephrine Hcl
Usage Information:
Do not use more than directeddo not take more than 12 caplets in any 24-hour periodadults and children 12 years and over: take 2 caplets every 4 hourschildren under 12 years: do not use
11-Digit NDC Billing Format:
49035035609
NDC to RxNorm Crosswalk:
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - APAP 325 MG / Diphenhydramine Hydrochloride 12.5 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Wal-mart Stores Inc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-23-2020
    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.

    Frequently Asked Questions

    What is NDC 49035-356-09?

    The NDC Packaged Code 49035-356-09 is assigned to a package of 1 kit in 1 carton * 10 tablet, film coated in 1 blister pack * 10 tablet, film coated in 1 blister pack of Day And Night Sinus, a human over the counter drug labeled by Wal-mart Stores Inc. The product's dosage form is kit and is administered via form.

    Is NDC 49035-356 included in the NDC Directory?

    Yes, Day And Night Sinus with product code 49035-356 is active and included in the NDC Directory. The product was first marketed by Wal-mart Stores Inc on October 23, 2020 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 49035-356-09?

    The 11-digit format is 49035035609. 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
    5-3-249035-356-095-4-249035-0356-09