Day-time Cold/flu Relief Liquid
NDC Package 53943-506-28
Package Information
Day-time Cold/flu Relief (acetaminophen, dextromethorphan hydrobromide, phenylephrine hcl) liquids is take only as recommended (see overdose warning)use dosage cup or tablespoon (TBSP)do not exceed 4 doses per 24 hours age dose adults and children 12 years and over 30 mL (2 TBSP) every 4 hours children 6 years to under 12 years 15 mL (1 TBSP) every 4 hours children 4 years to under 6 years ask a doctor children under 4 years do not use* When using Day Time and Night Time products, carefully read each label to ensure correct dosing. This formulation utilizes a liquid delivery system. Marketed by Discount Drug Mart, this product is identified by NDC 53943-506 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
- RxCUI: 1113705 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
- RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG per 15 ML Oral Solution
- RxCUI: 1113705 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG per 30 ML Oral Solution
- RxCUI: 1113705 - APAP 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
Clinical Specifications
- Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
- Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
- Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
- Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
- Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
- alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 53943 - Discount Drug Mart
- 53943-506 - Day-time Cold/flu Relief
- 53943-506-28 - 354 mL in 1 BOTTLE
- 53943-506 - Day-time Cold/flu Relief
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 53943-506-28 identifies a specific commercial package of 354 ml in 1 bottle of Day-time Cold/flu Relief, a human over the counter drug labeled by Discount Drug Mart. This liquid is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; phenylephrine hydrochloride 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 Discount Drug Mart on October 25, 2014. The current certification is valid through December 31, 2026.
How is this Discount Drug Mart product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 53943050628. 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.