Tussin Dm Max Daytime Nighttime Kit
NDC Package 69842-929-12
Package Information
Tussin Dm Max Daytime Nighttime (dextromethorphan hbr, doxylamine succinate, guaifesesin) kits 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 •do not take more than 6 doses in any 24-hour period•measure only with dosing cup provided•keep dosing cup with product•mL = milliliter•this adult product is not intended for use in children under 12 years of ageagedoseadults and children 12 years and over20 mL every 4 hourschildren under 12 yearsdo not use. This formulation utilizes a kit delivery system. Marketed by Cvs Pharmacy, this product is identified by NDC 69842-929 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution
- RxCUI: 1020138 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
- RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
- RxCUI: 1020138 - dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral Solution
- RxCUI: 1115329 - dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 20 mL Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69842 - Cvs Pharmacy
- 69842-929 - Tussin Dm Max Daytime Nighttime
- 69842-929-12 - 1 KIT in 1 CARTON * 1 BOTTLE in 1 CARTON (69842-699-26) / 118 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (69842-819-26) / 118 mL in 1 BOTTLE
- 69842-929 - Tussin Dm Max Daytime Nighttime
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 69842-929-12 identifies a specific commercial package of 1 kit in 1 carton * 1 bottle in 1 carton (69842-699-26) / 118 ml in 1 bottle * 1 bottle in 1 carton (69842-819-26) / 118 ml in 1 bottle of Tussin Dm Max Daytime Nighttime, a human over the counter drug labeled by Cvs Pharmacy. 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 Cvs Pharmacy on July 20, 2018. The current certification is valid through December 31, 2026.
How is this Cvs Pharmacy product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69842092912. 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.