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  5. NDC Package Code: 37000-934-48 Vicks Dayquil Severe And Vicks Nyquil Severe Cold And Flu

NDC Package 37000-934-48 Vicks Dayquil Severe And Vicks Nyquil Severe Cold And Flu

Acetaminophen,Phenylephrine Hydrochloride,Dextromethorphan Hydrobromide,Guaifenesin And - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

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:
37000-934-48
Package Description:
1 KIT in 1 PACKAGE * 1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
37000-934
Proprietary Name:
Vicks Dayquil Severe And Vicks Nyquil Severe Cold And Flu
Non-Proprietary Name:
Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, Guaifenesin And Doxylamine Succinate
Usage Information:
Take only as directeddo not exceed 8 LiquiCaps per 24 hrsadults & children 12 yrs & over 2 LiquiCaps with water every 4 hrs children 4 to under 12 yrs ask a doctor children under 4 yrs do not use take only as directeddo not exceed 8 LiquiCaps per 24 hoursadults & children 12 yrs & over 2 LiquiCaps with water every 4 hrschildren 4 to under 12 yrs ask a doctorchildren under 4 yrs do not use
11-Digit NDC Billing Format:
37000093448
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
    • Product Type:
    Human Otc Drug
    Labeler Name:
    The Procter & Gamble Manufacturing Company
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-04-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    37000-934-121 KIT in 1 PACKAGE * 1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    37000-934-241 KIT in 1 PACKAGE * 1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    37000-934-721 KIT in 1 PACKAGE * 1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 37000-934-48?

    The NDC Packaged Code 37000-934-48 is assigned to a package of 1 kit in 1 package * 1 blister pack in 1 carton / 8 capsule, liquid filled in 1 blister pack * 1 blister pack in 1 carton / 4 capsule, liquid filled in 1 blister pack of Vicks Dayquil Severe And Vicks Nyquil Severe Cold And Flu, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is kit and is administered via form.

    Is NDC 37000-934 included in the NDC Directory?

    Yes, Vicks Dayquil Severe And Vicks Nyquil Severe Cold And Flu with product code 37000-934 is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on July 04, 2019 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 37000-934-48?

    The 11-digit format is 37000093448. 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
    5-3-237000-934-485-4-237000-0934-48