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Daytime Multi-Symptom Severe Cold - 0363-0503-08 - (Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin)

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Drug Information of Daytime Multi-Symptom Severe Cold

Product NDC: 0363-0503
Proprietary Name: Daytime Multi-Symptom Severe Cold
Non Proprietary Name: Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin
Active Ingredient(s): 325; 10; 200; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Daytime Multi-Symptom Severe Cold

Product NDC: 0363-0503
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050804

Package Information of Daytime Multi-Symptom Severe Cold

Package NDC: 0363-0503-08
Package Description: 2 BLISTER PACK in 1 CARTON (0363-0503-08) > 12 TABLET, COATED in 1 BLISTER PACK

NDC Information of Daytime Multi-Symptom Severe Cold

NDC Code 0363-0503-08
Proprietary Name Daytime Multi-Symptom Severe Cold
Package Description 2 BLISTER PACK in 1 CARTON (0363-0503-08) > 12 TABLET, COATED in 1 BLISTER PACK
Product NDC 0363-0503
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20050804
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WALGREEN CO.
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 200; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Daytime Multi-Symptom Severe Cold


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