37000-415 NDC - VICKS DAYQUIL AND VICKS NYQUIL ()

Drug Information

Product NDC: 37000-415

Proprietary Name: Vicks DayQuil and Vicks NyQuil

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: The Procter & Gamble Manufacturing Company
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/21/2014

Package Information

No. Package Code Package Description Billing Unit
137000-415-241 KIT in 1 PACKAGE (37000-415-24) * 8 BLISTER PACK in 1 CARTON / 2 TABLET in 1 BLISTER PACK * 4 BLISTER PACK in 1 CARTON / 2 TABLET, COATED in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC37000-415The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEVicks DayQuil and Vicks NyQuilThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXSevere Cold and FluA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE7/21/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEThe Procter & Gamble Manufacturing CompanyName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023