Home > National Drug Code (NDC) > smart sense daytime

smart sense daytime - 49738-656-38 - (acetaminophen, dextromethorphan Hbr, Phenylephrine HCl)

Alphabetical Index


Drug Information of smart sense daytime

Product NDC: 49738-656
Proprietary Name: smart sense 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 smart sense daytime

Product NDC: 49738-656
Labeler Name: Kmart Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110201

Package Information of smart sense daytime

Package NDC: 49738-656-38
Package Description: 296 mL in 1 BOTTLE (49738-656-38)

NDC Information of smart sense daytime

NDC Code 49738-656-38
Proprietary Name smart sense daytime
Package Description 296 mL in 1 BOTTLE (49738-656-38)
Product NDC 49738-656
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kmart Corporation
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 smart sense daytime


General Information