Maximum Strength Daytime Nighttime Cold And Flu Kit
NDC Package 69842-451-24

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Maximum Strength Daytime Nighttime Cold And Flu (acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl) kits is usestemporarily relieves these common cold and flu symptoms:sinus congestion and pressure cough minor aches and pains headache nasal congestion sore throat runny nose and sneezing ( Nighttime only) itchy, watery eyes due to hay fever ( Nighttime only) itching of the nose or throat ( Nighttime only) helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive ( Daytime only) controls cough to help you get to sleeptemporarily reduces fever. This formulation utilizes a kit delivery system. Marketed by Cvs Pharmacy, Inc., this product is identified by NDC 69842-451 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
69842-451-24
Package Description
1 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK * 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-094-16) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-382-08)
Product Code
11-Digit Billing Format
69842045124
RxNorm Crosswalk
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1297288 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / doxylamine succinate 6.25 MG / Phenylephrine Hydrochloride 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Capsule

Clinical Specifications

Proprietary Name
Maximum Strength Daytime Nighttime Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, Phenylephrine Hcl
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Usestemporarily relieves these common cold and flu symptoms:sinus congestion and pressure cough minor aches and pains headache nasal congestion sore throat runny nose and sneezing ( Nighttime only) itchy, watery eyes due to hay fever ( Nighttime only) itching of the nose or throat ( Nighttime only) helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive ( Daytime only) controls cough to help you get to sleeptemporarily reduces fever

Regulatory & Marketing

Labeler Name
Cvs Pharmacy, Inc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-10-2021
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 69842-451-24 identifies a specific commercial package of 1 blister pack in 1 carton / 1 kit in 1 blister pack * 16 capsule, liquid filled in 1 blister pack (69842-094-16) * 8 capsule, liquid filled in 1 blister pack (69842-382-08) of Maximum Strength Daytime Nighttime Cold And Flu, a human over the counter drug labeled by Cvs Pharmacy, 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 Cvs Pharmacy, Inc. on July 10, 2021. The current certification is valid through December 31, 2027.

How is this Cvs Pharmacy, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69842045124. 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:

10-Digit Format (5-3-2)
69842-451-24
11-Digit CMS (5-4-2)
69842-0451-24

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.