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Daytime Nitetime - 41250-926-01 - (Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl)

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Drug Information of Daytime Nitetime

Product NDC: 41250-926
Proprietary Name: Daytime 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 Nitetime

Product NDC: 41250-926
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20061108

Package Information of Daytime Nitetime

Package NDC: 41250-926-01
Package Description: 1 KIT in 1 PACKAGE (41250-926-01) * 296 mL in 1 BOTTLE (41250-041-38) * 296 mL in 1 BOTTLE (41250-656-38)

NDC Information of Daytime Nitetime

NDC Code 41250-926-01
Proprietary Name Daytime Nitetime
Package Description 1 KIT in 1 PACKAGE (41250-926-01) * 296 mL in 1 BOTTLE (41250-041-38) * 296 mL in 1 BOTTLE (41250-656-38)
Product NDC 41250-926
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 20061108
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Meijer Distribution Inc
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Daytime Nitetime


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