Day Time - 63941-142-06 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of Day Time

Product NDC: 63941-142
Proprietary Name: 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 Day Time

Product NDC: 63941-142
Labeler Name: Best Choice
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090813

Package Information of Day Time

Package NDC: 63941-142-06
Package Description: 177 mL in 1 BOTTLE, PLASTIC (63941-142-06)

NDC Information of Day Time

NDC Code 63941-142-06
Proprietary Name Day Time
Package Description 177 mL in 1 BOTTLE, PLASTIC (63941-142-06)
Product NDC 63941-142
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090813
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Best Choice
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 Day Time


General Information