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Daytime Cold and Flu Relief - 62211-339-09 - (Acetaminophen, Dextromethorphan HBr, Phenylephrine HCI)

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Drug Information of Daytime Cold and Flu Relief

Product NDC: 62211-339
Proprietary Name: Daytime Cold and Flu Relief
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Phenylephrine HCI
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan HBr, Phenylephrine HCI
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Daytime Cold and Flu Relief

Product NDC: 62211-339
Labeler Name: A&Z Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110609

Package Information of Daytime Cold and Flu Relief

Package NDC: 62211-339-09
Package Description: 1 BLISTER PACK in 1 BOX (62211-339-09) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Daytime Cold and Flu Relief

NDC Code 62211-339-09
Proprietary Name Daytime Cold and Flu Relief
Package Description 1 BLISTER PACK in 1 BOX (62211-339-09) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 62211-339
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Phenylephrine HCI
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20110609
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name A&Z Pharmaceutical, Inc.
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Daytime Cold and Flu Relief


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