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  5. NDC Package Code: 69842-071-04 Maximum Strength Nighttime Cold/flu Relief

NDC Package 69842-071-04 Maximum Strength Nighttime Cold/flu Relief

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
69842-071-04
Package Description:
2 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
69842-071
Proprietary Name:
Maximum Strength Nighttime Cold/flu Relief
Usage Information:
Take only as directed - see Overdose Warningdo not exceed 4 doses per 24 hrsadults & children 12 yrs and over        2 softgels with water every 4 hrschildren 4 to under 12 yrs         ask a doctorchildren under 4 yrs         do not usewhen using other Nighttime or Daytime products, carefully read each label to ensure correct dosing
11-Digit NDC Billing Format:
69842007104
NDC to 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
Labeler Name:
Cvs Pharmacy, Inc.
Sample Package:
No
FDA Application Number:
part341
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
12-14-2016
Listing Expiration Date:
12-31-2024
Exclude Flag:
I
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 69842-071-04?

The NDC Packaged Code 69842-071-04 is assigned to a package of 2 blister pack in 1 carton / 12 capsule, liquid filled in 1 blister pack of Maximum Strength Nighttime Cold/flu Relief, labeled by Cvs Pharmacy, Inc.. The product's dosage form is and is administered via form.

Is NDC 69842-071 included in the NDC Directory?

No, Maximum Strength Nighttime Cold/flu Relief with product code 69842-071 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Cvs Pharmacy, Inc. on December 14, 2016 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 69842-071-04?

The 11-digit format is 69842007104. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-269842-071-045-4-269842-0071-04