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cold relief - 37808-250-04 - (Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl)

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Drug Information of cold relief

Product NDC: 37808-250
Proprietary Name: cold relief
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 cold relief

Product NDC: 37808-250
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090211

Package Information of cold relief

Package NDC: 37808-250-04
Package Description: 1 KIT in 1 CARTON (37808-250-04) * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of cold relief

NDC Code 37808-250-04
Proprietary Name cold relief
Package Description 1 KIT in 1 CARTON (37808-250-04) * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 37808-250
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 20090211
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of cold relief


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