Home > National Drug Code (NDC) > Flu Relief Therapy Day Time

Flu Relief Therapy Day Time - 11822-2104-8 - (Acetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of Flu Relief Therapy Day Time

Product NDC: 11822-2104
Proprietary Name: Flu Relief Therapy Day Time
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/15mL; mg/15mL; mg/15mL & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Flu Relief Therapy Day Time

Product NDC: 11822-2104
Labeler Name: Rite Aid
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090904

Package Information of Flu Relief Therapy Day Time

Package NDC: 11822-2104-8
Package Description: 245 mL in 1 BOTTLE, PLASTIC (11822-2104-8)

NDC Information of Flu Relief Therapy Day Time

NDC Code 11822-2104-8
Proprietary Name Flu Relief Therapy Day Time
Package Description 245 mL in 1 BOTTLE, PLASTIC (11822-2104-8)
Product NDC 11822-2104
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090904
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rite Aid
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 Flu Relief Therapy Day Time


General Information