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Severe Cold Multi-Symptom - 49035-503-08 - (Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin)

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Drug Information of Severe Cold Multi-Symptom

Product NDC: 49035-503
Proprietary Name: Severe Cold Multi-Symptom
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 Severe Cold Multi-Symptom

Product NDC: 49035-503
Labeler Name: Wal-Mart Stores Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050804

Package Information of Severe Cold Multi-Symptom

Package NDC: 49035-503-08
Package Description: 1 BLISTER PACK in 1 CARTON (49035-503-08) > 24 TABLET, COATED in 1 BLISTER PACK

NDC Information of Severe Cold Multi-Symptom

NDC Code 49035-503-08
Proprietary Name Severe Cold Multi-Symptom
Package Description 1 BLISTER PACK in 1 CARTON (49035-503-08) > 24 TABLET, COATED in 1 BLISTER PACK
Product NDC 49035-503
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 Wal-Mart Stores Inc
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 Severe Cold Multi-Symptom


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