Tussin Dm Nighttime Max Solution
NDC Package 42507-689-26
Package Information
Tussin Dm Nighttime Max (dextromethorphan hydrobromide, doxylamine succinate) solution is •measure only with dosing cup provided•keep dosing cup with product•mL = milliliter•do not take more than 4 doses in any 24-hour period•this adult product is not intended for use in children under 12 years of ageagedoseadults and children 12 years and over20 mL every 6 hourschildren under 12 yearsdo not use. This formulation utilizes a solution delivery system. Marketed by Hyvee Inc, this product is identified by NDC 42507-689 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1115329 - dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 20 mL Oral Solution
- RxCUI: 1115329 - dextromethorphan hydrobromide 1.5 MG/ML / doxylamine succinate 0.625 MG/ML Oral Solution
- RxCUI: 1115329 - dextromethorphan hydrobromide 30 MG / doxylamine succinate 12.5 MG per 20 ML Oral Solution
- RxCUI: 1115329 - dextromethorphan hydrobromide 7.5 MG / doxylamine succinate 3.125 MG per 5 ML Oral Solution
Clinical Specifications
- Antihistamine - [EPC] (Established Pharmacologic Class)
- Histamine Receptor Antagonists - [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)
Regulatory & Marketing
Hierarchy Structure
- 42507 - Hyvee Inc
- 42507-689 - Tussin Dm Nighttime Max
- 42507-689-26 - 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE (42507-689-00)
- 42507-689 - Tussin Dm Nighttime Max
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 42507-689-26 identifies a specific commercial package of 1 bottle in 1 carton / 118 ml in 1 bottle (42507-689-00) of Tussin Dm Nighttime Max, a human over the counter drug labeled by Hyvee Inc. This solution is formulated for oral use and contains dextromethorphan hydrobromide; doxylamine succinate 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 Hyvee Inc on January 13, 2026. The current certification is valid through December 31, 2027.
How is this Hyvee Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 42507068926. 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.