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daytime pe nitetime - 56062-090-57 - (Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl)

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Drug Information of daytime pe nitetime

Product NDC: 56062-090
Proprietary Name: daytime pe nitetime
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl
Active Ingredient(s):    & nbsp;   Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of daytime pe nitetime

Product NDC: 56062-090
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121029

Package Information of daytime pe nitetime

Package NDC: 56062-090-57
Package Description: 1 KIT in 1 CARTON (56062-090-57) * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of daytime pe nitetime

NDC Code 56062-090-57
Proprietary Name daytime pe nitetime
Package Description 1 KIT in 1 CARTON (56062-090-57) * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 56062-090
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl
Dosage Form Name KIT
Route Name
Start Marketing Date 20121029
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Publix Super Markets Inc
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of daytime pe nitetime


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