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  5. NDC Package Code: 36800-765-12 Sinus Max Relief Day And Night

NDC Package 36800-765-12 Sinus Max Relief Day And Night

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:
36800-765-12
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:
36800-765
Proprietary Name:
Sinus Max Relief Day And Night
Usage Information:
Do not take more than directed (see Overdose warning)do not take more than 12 softgels in any 24-hour periodadults and children 12 years of age and older: take 2 softgels every 4 hourschildren under 12 years of age: do not use
11-Digit NDC Billing Format:
36800076512
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
  • 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
    • Labeler Name:
    Topco Associates Llc
    Sample Package:
    No
    Start Marketing Date:
    05-01-2021
    Listing Expiration Date:
    12-31-2022
    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 36800-765-12?

    The NDC Packaged Code 36800-765-12 is assigned to a package of 1 kit in 1 carton * 8 capsule, liquid filled in 1 blister pack * 4 capsule, liquid filled in 1 blister pack of Sinus Max Relief Day And Night, labeled by Topco Associates Llc. The product's dosage form is and is administered via form.

    Is NDC 36800-765 included in the NDC Directory?

    No, Sinus Max Relief Day And Night with product code 36800-765 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Topco Associates Llc on May 01, 2021 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 36800-765-12?

    The 11-digit format is 36800076512. 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
    5-3-236800-765-125-4-236800-0765-12