Maximum Strength Sinus Relief Day And Night Softgels - 24 Ct Kit
NDC Package 76162-679-24

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Maximum Strength Sinus Relief Day And Night Softgels - 24 Ct (acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, phenylephrine hydrochloride) kits is • do not take more than directed (see Overdose warning)• do not take more than 12 softgels in any 24-hour period• adults and children 12 years of age and older: take 2 softgels every 4 hours• children under 12 years of age: do not use. This formulation utilizes a kit delivery system. Marketed by Topco Associates Llc, this product is identified by NDC 76162-679 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
76162-679-24
Package Description
1 KIT in 1 CARTON * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
76162-679
11-Digit Billing Format
76162067924
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 Sinus Relief Day And Night Softgels - 24 Ct
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, Phenylephrine Hydrochloride
Dosage Form
Kit - A packaged collection of related material.
Usage Information
• do not take more than directed (see Overdose warning)• do not take more than 12 softgels in any 24-hour period• adults and children 12 years of age and older: take 2 softgels every 4 hours• children under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Topco Associates Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-13-2025
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 76162-679-24 identifies a specific commercial package of 1 kit in 1 carton * 8 capsule, liquid filled in 1 blister pack * 4 capsule, liquid filled in 1 blister pack of Maximum Strength Sinus Relief Day And Night Softgels - 24 Ct, a human over the counter drug labeled by Topco Associates Llc. 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 Topco Associates Llc on October 13, 2025. The current certification is valid through December 31, 2026.

How is this Topco Associates Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76162067924. 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)
76162-679-24
11-Digit CMS (5-4-2)
76162-0679-24

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