Sinus Pressure And Congestion Relief Kit
NDC Package 11822-9485-9

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

Package Information

Sinus Pressure And Congestion Relief (diphenhydramine hcl, phenylephrine hcl) kits is adults and children 12 years and overtake 1 tablet every 4 hoursdo not take more than 6 tablets in 24 hourschildren under 12 years: ask a doctor. This formulation utilizes a kit delivery system. Marketed by Rite Aid Corporation, this product is identified by NDC 11822-9485 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
11822-9485-9
Package Description
1 KIT in 1 CARTON * 12 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
Product Code
11-Digit Billing Format
11822948509
RxNorm Crosswalk
  • RxCUI: 1049182 - phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1049182 - phenylephrine hydrochloride 10 MG Oral Tablet
  • RxCUI: 1052928 - diphenhydrAMINE HCl 25 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1052928 - diphenhydramine hydrochloride 25 MG / phenylephrine hydrochloride 10 MG Oral Tablet
  • RxCUI: 2639176 - {1 (diphenhydramine hydrochloride 25 MG / phenylephrine hydrochloride 10 MG Oral Tablet) / 1 (phenylephrine hydrochloride 10 MG Oral Tablet) } Pack

Clinical Specifications

Proprietary Name
Sinus Pressure And Congestion Relief
Non-Proprietary Name
Diphenhydramine Hcl, Phenylephrine Hcl
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Adults and children 12 years and overtake 1 tablet every 4 hoursdo not take more than 6 tablets in 24 hourschildren under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Rite Aid Corporation
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-02-2019
Listing Expiration
12-31-2026
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 11822-9485-9 identifies a specific commercial package of 1 kit in 1 carton * 12 tablet, film coated in 1 blister pack * 8 tablet, film coated in 1 blister pack of Sinus Pressure And Congestion Relief, a human over the counter drug labeled by Rite Aid Corporation. 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 Rite Aid Corporation on July 02, 2019. The current certification is valid through December 31, 2026.

How is this Rite Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11822948509. 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 (5-4-1)
11822-9485-9
11-Digit CMS (5-4-2)
11822-9485-09

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