DayTime - 37808-656-40 - (acetaminophen, dextromethorphan Hbr, Phenylephrine HCl)

Alphabetical Index


Drug Information of DayTime

Product NDC: 37808-656
Proprietary Name: DayTime
Non Proprietary Name: acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Active Ingredient(s): 325; 10; 5    mg/15mL; mg/15mL; mg/15mL & nbsp;   acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of DayTime

Product NDC: 37808-656
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060802

Package Information of DayTime

Package NDC: 37808-656-40
Package Description: 354 mL in 1 BOTTLE (37808-656-40)

NDC Information of DayTime

NDC Code 37808-656-40
Proprietary Name DayTime
Package Description 354 mL in 1 BOTTLE (37808-656-40)
Product NDC 37808-656
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20060802
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
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 DayTime


General Information