Daytime Cold And Flu Nighttime Cold And Flu Kit
NDC Package 79481-5200-0
Package Information
Daytime Cold And Flu Nighttime Cold And Flu (acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, doxylamine succinate) kits is •take only as directed - see overdose warning•do not exceed 8 caplets per 24 hrsadults & children 12 yrs & over2 caplets with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use •take only as directed - see overdose warning•do not exceed 8 caplets per 24 hrsadults & children 12 yrs & over2 caplets with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use. This formulation utilizes a kit delivery system. Marketed by Meijer, Inc., this product is identified by NDC 79481-5200 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 79481 - Meijer, Inc.
- 79481-5200 - Daytime Cold And Flu Nighttime Cold And Flu
- 79481-5200-0 - 1 KIT in 1 CARTON * 2 TABLET, FILM COATED in 1 BLISTER PACK (41250-569-00) * 2 TABLET, FILM COATED in 1 BLISTER PACK (79481-0099-0)
- 79481-5200 - Daytime Cold And Flu Nighttime Cold And Flu
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 full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 79481-5200-0 identifies a specific commercial package of 1 kit in 1 carton * 2 tablet, film coated in 1 blister pack (41250-569-00) * 2 tablet, film coated in 1 blister pack (79481-0099-0) of Daytime Cold And Flu Nighttime Cold And Flu, a human over the counter drug labeled by Meijer, Inc.. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Meijer, Inc. on August 21, 2021. The current certification is valid through December 31, 2026.
How is this Meijer, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481520000. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.
