Home > National Drug Code (NDC) > smart sense tussin dm

smart sense tussin dm - 49738-359-26 - (Dextromethorphan Hydrobromide, Guaifenesin)

Alphabetical Index


Drug Information of smart sense tussin dm

Product NDC: 49738-359
Proprietary Name: smart sense tussin dm
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of smart sense tussin dm

Product NDC: 49738-359
Labeler Name: Kmart Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20101017

Package Information of smart sense tussin dm

Package NDC: 49738-359-26
Package Description: 1 BOTTLE in 1 CARTON (49738-359-26) > 118 mL in 1 BOTTLE

NDC Information of smart sense tussin dm

NDC Code 49738-359-26
Proprietary Name smart sense tussin dm
Package Description 1 BOTTLE in 1 CARTON (49738-359-26) > 118 mL in 1 BOTTLE
Product NDC 49738-359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101017
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kmart Corporation
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of smart sense tussin dm


General Information