Adult Severe Congestion And Cough
NDC Package 49348-083-36
Package Information
Adult Severe Congestion And Cough is do not take more than 6 doses in 24-hour periodmeasure only with dosing coup provideddo not use dosing cup with other productsdose as follows or as directed by a doctorAdults and children 12 years and older: 20 mL in dosing cup provided every 4 hoursChildren under 12 years of age: Do not use. Marketed by Mckesson, this product is identified by NDC 49348-083 and is authorized under FDA application part341.
Identification & Billing
- RxCUI: 1043543 - dextromethorphan HBr 5 MG / guaiFENesin 100 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution
- RxCUI: 1043543 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
- RxCUI: 1043543 - dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
- RxCUI: 1043543 - dextromethorphan HBr 5 MG / guaifenesin 100 MG / phenylephrine HCl 2.5 MG per 5 ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 49348 - Mckesson
- 49348-083 - Adult Severe Congestion And Cough
- 49348-083-36 - 177 mL in 1 BOTTLE
- 49348-083 - Adult Severe Congestion 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 49348-083-36 identifies a specific commercial package of 177 ml in 1 bottle of Adult Severe Congestion And Cough, labeled by Mckesson. This product is billed per "ML" milliliter and contains an estimated amount of 177 billable units per package. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Mckesson on December 01, 2012. The current certification is valid through December 31, 2019.
How is this Mckesson product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 49348008336. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 177 total billable units per package. 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.
