NDC Package 70692-103-12 Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime

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:
70692-103-12
Package Description:
1 KIT in 1 PACKAGE, COMBINATION * 8 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime
Usage Information:
* temporarily relieves:nasal congestionheadacheminor aches and painsinus congestion and pressurerunny nose and sneezing (Nighttime only)cough (Nighttime only)* temporarily promotes nasal and/or sinus drainag* helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive (Daytime only)
11-Digit NDC Billing Format:
70692010312
NDC to RxNorm Crosswalk:
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1233575 - APAP 325 MG / Diphenhydramine Hydrochloride 12.5 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • Labeler Name:
    Strive Pharmaceuticals Inc.
    Sample Package:
    No
    Start Marketing Date:
    03-01-2018
    Listing Expiration Date:
    12-31-2021
    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 70692-103-12?

    The NDC Packaged Code 70692-103-12 is assigned to a package of 1 kit in 1 package, combination * 8 tablet, film coated in 1 blister pack * 4 tablet, film coated in 1 blister pack of Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime, labeled by Strive Pharmaceuticals Inc.. The product's dosage form is and is administered via form.

    Is NDC 70692-103 included in the NDC Directory?

    No, Multi Symptom Sinus Relief Pain And Congestion Daytime Nighttime with product code 70692-103 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Strive Pharmaceuticals Inc. on March 01, 2018 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70692-103-12?

    The 11-digit format is 70692010312. 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
    5-3-270692-103-125-4-270692-0103-12