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  5. NDC Package Code: 11822-0677-8 Severe Nighttime Cold And Flu Relief

NDC Package 11822-0677-8 Severe Nighttime Cold And Flu Relief

Acetaminophen,Dextromethorphan Hbr,Doxylamine Succinate,Phenylephrine Hcl Tablet, Film - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
11822-0677-8
Package Description:
2 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
11822-0677
Proprietary Name:
Severe Nighttime Cold And Flu Relief
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, Phenylephrine Hcl
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Doxylamine Succinate; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directeddo not take more than 8 caplets in 24 hoursadults and children 12 years and over: take 2 caplets with water every 4 hourschildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
11822067708
NDC to RxNorm Crosswalk:
  • RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1546881 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / doxylamine succinate 6.25 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Rite Aid Corporation
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
12-10-2019
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
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 11822-0677-8?

The NDC Packaged Code 11822-0677-8 is assigned to a package of 2 blister pack in 1 carton / 12 tablet, film coated in 1 blister pack of Severe Nighttime Cold And Flu Relief, a human over the counter drug labeled by Rite Aid Corporation. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 11822-0677 included in the NDC Directory?

Yes, Severe Nighttime Cold And Flu Relief with product code 11822-0677 is active and included in the NDC Directory. The product was first marketed by Rite Aid Corporation on December 10, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 11822-0677-8?

The 11-digit format is 11822067708. 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 5-4-1 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
5-4-111822-0677-85-4-211822-0677-08