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Vicks DayQuil - 37000-555-08 - (Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride)

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Drug Information of Vicks DayQuil

Product NDC: 37000-555
Proprietary Name: Vicks DayQuil
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/15mL; mg/15mL; mg/15mL & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Vicks DayQuil

Product NDC: 37000-555
Labeler Name: The Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110622

Package Information of Vicks DayQuil

Package NDC: 37000-555-08
Package Description: 236 mL in 1 BOTTLE, PLASTIC (37000-555-08)

NDC Information of Vicks DayQuil

NDC Code 37000-555-08
Proprietary Name Vicks DayQuil
Package Description 236 mL in 1 BOTTLE, PLASTIC (37000-555-08)
Product NDC 37000-555
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110622
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name The Procter & Gamble Manufacturing Company
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/15mL; mg/15mL; mg/15mL
Pharmaceutical Classes

Complete Information of Vicks DayQuil


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