NDC Package 11822-8557-0 Day Maximum Strength Cold And Flu Relief

View Billable Units, 11-Digit Format, RxNorm

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:
11822-8557-0
Package Description:
1 KIT in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (11822-3856-8) * 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (11822-3855-9)
Product Code:
Proprietary Name:
Day Maximum Strength Cold And Flu Relief
Usage Information:
Temporarily relieves these symptoms due to a cold or flu: minor aches and pains · headache · cough · sore throat · nasal and sinus congestiontemporarily reduces fever temporarily relieves these symptoms due to a cold or flu:minor aches and pains, headache, nasal and sinus congestion, cough, sore throat, runny nose, sneezingtemporarily reduces fever
11-Digit NDC Billing Format:
11822855700
NDC to RxNorm Crosswalk:
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • 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
Labeler Name:
Rite Aid
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:
08-03-2020
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 11822-8557-0?

The NDC Packaged Code 11822-8557-0 is assigned to a package of 1 kit in 1 blister pack * 8 capsule, liquid filled in 1 blister pack (11822-3856-8) * 16 capsule, liquid filled in 1 blister pack (11822-3855-9) of Day Maximum Strength Cold And Flu Relief, labeled by Rite Aid. The product's dosage form is and is administered via form.

Is NDC 11822-8557 included in the NDC Directory?

No, Day Maximum Strength Cold And Flu Relief with product code 11822-8557 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rite Aid on August 03, 2020 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 11822-8557-0?

The 11-digit format is 11822855700. 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
5-4-111822-8557-05-4-211822-8557-00