DayQuil - 66715-9708-1 - (Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of DayQuil

Product NDC: 66715-9708
Proprietary Name: DayQuil
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of DayQuil

Product NDC: 66715-9708
Labeler Name: Lil' Drug Store Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100916

Package Information of DayQuil

Package NDC: 66715-9708-1
Package Description: 1 POUCH in 1 CARTON (66715-9708-1) > 2 CAPSULE, LIQUID FILLED in 1 POUCH

NDC Information of DayQuil

NDC Code 66715-9708-1
Proprietary Name DayQuil
Package Description 1 POUCH in 1 CARTON (66715-9708-1) > 2 CAPSULE, LIQUID FILLED in 1 POUCH
Product NDC 66715-9708
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20100916
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Lil' Drug Store Products, Inc.
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of DayQuil


General Information