Maximum Strength Non Drowsy Day And Night Cold And Flu Kit
NDC Package 49035-674-16
Package Information
Maximum Strength Non Drowsy Day And Night Cold And Flu kits is directions· do not take more than the recommended dose· adults and children 12 years and over: take 2 capsules with water every 4 hours. This formulation utilizes a kit delivery system. Marketed by Wal-mart Stores Inc, this product is identified by NDC 49035-674 and is authorized under FDA application M012.
Identification & Billing
- 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: 1297288 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Capsule
- RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 49035 - Wal-mart Stores Inc
- 49035-674 - Maximum Strength Non Drowsy Day And Night Cold And Flu
- 49035-674-16 - 1 KIT in 1 CARTON * 1 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-245-12) * 1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-246-04)
- 49035-674 - Maximum Strength Non Drowsy Day And Night 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 49035-674-16 identifies a specific commercial package of 1 kit in 1 carton * 1 blister pack in 1 carton / 12 capsule, liquid filled in 1 blister pack (79903-245-12) * 1 blister pack in 1 carton / 4 capsule, liquid filled in 1 blister pack (79903-246-04) of Maximum Strength Non Drowsy Day And Night Cold And Flu, a human over the counter drug labeled by Wal-mart Stores 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 Wal-mart Stores Inc on November 16, 2020. The current certification is valid through December 31, 2027.
How is this Wal-mart Stores Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 49035067416. 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 Product segment to maintain the 5-4-2 structure.