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Multi Sympton Cold Day Night - 67510-0156-2 - (Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl)

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Drug Information of Multi Sympton Cold Day Night

Product NDC: 67510-0156
Proprietary Name: Multi Sympton Cold Day Night
Non Proprietary Name: Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Active Ingredient(s):    & nbsp;   Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Multi Sympton Cold Day Night

Product NDC: 67510-0156
Labeler Name: Kareway Product, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120501

Package Information of Multi Sympton Cold Day Night

Package NDC: 67510-0156-2
Package Description: 1 KIT in 1 PACKAGE, COMBINATION (67510-0156-2) * 1 BLISTER PACK in 1 BOX (67510-1156-1) > 12 TABLET in 1 BLISTER PACK * 1 BLISTER PACK in 1 BOX (67510-2156-1) > 12 TABLET in 1 BLISTER PACK

NDC Information of Multi Sympton Cold Day Night

NDC Code 67510-0156-2
Proprietary Name Multi Sympton Cold Day Night
Package Description 1 KIT in 1 PACKAGE, COMBINATION (67510-0156-2) * 1 BLISTER PACK in 1 BOX (67510-1156-1) > 12 TABLET in 1 BLISTER PACK * 1 BLISTER PACK in 1 BOX (67510-2156-1) > 12 TABLET in 1 BLISTER PACK
Product NDC 67510-0156
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Dosage Form Name KIT
Route Name
Start Marketing Date 20120501
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kareway Product, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Multi Sympton Cold Day Night


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