day time - 37808-994-60 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of day time

Product NDC: 37808-994
Proprietary Name: day time
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of day time

Product NDC: 37808-994
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110727

Package Information of day time

Package NDC: 37808-994-60
Package Description: 2 BLISTER PACK in 1 CARTON (37808-994-60) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of day time

NDC Code 37808-994-60
Proprietary Name day time
Package Description 2 BLISTER PACK in 1 CARTON (37808-994-60) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 37808-994
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20110727
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/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of day time


General Information