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Vicks DayQuil - 37000-690-12 - (Dextromethorphan Hydrobromide and Guaifenesin)

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Drug Information of Vicks DayQuil

Product NDC: 37000-690
Proprietary Name: Vicks DayQuil
Non Proprietary Name: Dextromethorphan Hydrobromide and Guaifenesin
Active Ingredient(s): 10; 200    mg/15mL; mg/15mL & nbsp;   Dextromethorphan Hydrobromide and Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Vicks DayQuil

Product NDC: 37000-690
Labeler Name: Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090714

Package Information of Vicks DayQuil

Package NDC: 37000-690-12
Package Description: 354 mL in 1 BOTTLE, PLASTIC (37000-690-12)

NDC Information of Vicks DayQuil

NDC Code 37000-690-12
Proprietary Name Vicks DayQuil
Package Description 354 mL in 1 BOTTLE, PLASTIC (37000-690-12)
Product NDC 37000-690
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide and Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090714
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Procter & Gamble Manufacturing Company
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 200
Strength Unit mg/15mL; mg/15mL
Pharmaceutical Classes

Complete Information of Vicks DayQuil


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