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Multi-Symptom Daytime Cold - 11673-560-08 - (Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr)

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Drug Information of Multi-Symptom Daytime Cold

Product NDC: 11673-560
Proprietary Name: Multi-Symptom Daytime Cold
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 Multi-Symptom Daytime Cold

Product NDC: 11673-560
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20080329

Package Information of Multi-Symptom Daytime Cold

Package NDC: 11673-560-08
Package Description: 1 BLISTER PACK in 1 CARTON (11673-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Multi-Symptom Daytime Cold

NDC Code 11673-560-08
Proprietary Name Multi-Symptom Daytime Cold
Package Description 1 BLISTER PACK in 1 CARTON (11673-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 11673-560
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 Target Corporation
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 Multi-Symptom Daytime Cold


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