NDC Package 79481-0888-8 Meijer Daytime Nighttime Cold And Flu Softgel

Acetaminophen,Dextromethorphan Hydrobromide,Doxylamine Succinate,Phenylephrine - 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:
79481-0888-8
Package Description:
1 KIT in 1 CARTON * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Meijer Daytime Nighttime Cold And Flu Softgel
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride
Usage Information:
• take only as directed• do not exceed 8 softgels per 24 hrs adults & children 12 yrs & over 2 softgels with water every 4 hrs  children 4 to under 12 yrs ask a doctor  children under 4 yrs do not use  • take only as directed• do not exceed 8 softgels per 24 hrs adults & children 12 yrs & over 2 softgels with water every 6 hrs  children 4 to under 12 yrs ask a doctor  children under 4 yrs do not use 
11-Digit NDC Billing Format:
79481088808
NDC to RxNorm Crosswalk:
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule
Product Type:
Human Otc Drug
Labeler Name:
Meijer, Inc.
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
07-31-2025
Listing Expiration Date:
12-31-2026
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 79481-0888-8?

The NDC Packaged Code 79481-0888-8 is assigned to a package of 1 kit in 1 carton * 8 capsule, liquid filled in 1 blister pack * 4 capsule, liquid filled in 1 blister pack of Meijer Daytime Nighttime Cold And Flu Softgel, a human over the counter drug labeled by Meijer, Inc.. The product's dosage form is kit and is administered via form.

Is NDC 79481-0888 included in the NDC Directory?

Yes, Meijer Daytime Nighttime Cold And Flu Softgel with product code 79481-0888 is active and included in the NDC Directory. The product was first marketed by Meijer, Inc. on July 31, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 79481-0888-8?

The 11-digit format is 79481088808. 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
5-4-179481-0888-85-4-279481-0888-08