Multi Symptom Severe Cold And Nighttime Severe Cold And Cough Kit
NDC Package 49035-948-12
Package Information
Multi Symptom Severe Cold And Nighttime Severe Cold And Cough (acetaminophen, dextromethorphan hbr, diphenhydramine hcl, phenylephrine hcl) kits is •do not use more than directed•take every 4 hours, while symptoms persist .do not take more than 6 packets in 24 hours unless directed by a doctorAgeDoseAdults and children 12 years of age One packetChildren under 12 years of ageDo not use•dissolve contents of one packet into 8 oz. This formulation utilizes a kit delivery system. Marketed by Wal-mart Stores Inc, this product is identified by NDC 49035-948 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
- RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
- RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Packet for Oral Solution
- RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Powder for Oral Solution
- RxCUI: 1189316 - APAP 500 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 49035 - Wal-mart Stores Inc
- 49035-948 - Multi Symptom Severe Cold And Nighttime Severe Cold And Cough
- 49035-948-12 - 1 KIT in 1 CARTON * 6 PACKET in 1 CARTON (79903-541-01) / 1 POWDER, FOR SOLUTION in 1 PACKET * 6 PACKET in 1 CARTON (79903-547-01) / 1 POWDER, FOR SOLUTION in 1 PACKET
- 49035-948 - Multi Symptom Severe Cold And Nighttime Severe Cold And Cough
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 49035-948-12 identifies a specific commercial package of 1 kit in 1 carton * 6 packet in 1 carton (79903-541-01) / 1 powder, for solution in 1 packet * 6 packet in 1 carton (79903-547-01) / 1 powder, for solution in 1 packet of Multi Symptom Severe Cold And Nighttime Severe Cold And Cough, 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 July 01, 2019. The current certification is valid through December 31, 2026.
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: 49035094812. 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.
