Daytime - 50804-470-24 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of Daytime

Product NDC: 50804-470
Proprietary Name: Daytime
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 Daytime

Product NDC: 50804-470
Labeler Name: Geiss, Destin & Dunn, Inc (Goodsense)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110729

Package Information of Daytime

Package NDC: 50804-470-24
Package Description: 2 BLISTER PACK in 1 CARTON (50804-470-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Daytime

NDC Code 50804-470-24
Proprietary Name Daytime
Package Description 2 BLISTER PACK in 1 CARTON (50804-470-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 50804-470
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 20110729
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Geiss, Destin & Dunn, Inc (Goodsense)
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 Daytime


General Information