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Cold Multi-Symptom Daytime - 55315-560-08 - (Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr)

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Drug Information of Cold Multi-Symptom Daytime

Product NDC: 55315-560
Proprietary Name: Cold Multi-Symptom Daytime
Non Proprietary Name: Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Cold Multi-Symptom Daytime

Product NDC: 55315-560
Labeler Name: FRED'S, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20080329

Package Information of Cold Multi-Symptom Daytime

Package NDC: 55315-560-08
Package Description: 1 BLISTER PACK in 1 CARTON (55315-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Cold Multi-Symptom Daytime

NDC Code 55315-560-08
Proprietary Name Cold Multi-Symptom Daytime
Package Description 1 BLISTER PACK in 1 CARTON (55315-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 55315-560
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20080329
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name FRED'S, INC.
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 Cold Multi-Symptom Daytime


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